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What is calcium Citrate and Vitamin D3 Tablets used for?

In the pharmaceutical industry, the combination of Calcium Citrate and Vitamin D3 (Cholecalciferol) is a premium mineral-vitamin supplement used to manage bone density and calcium homeostasis. As a pharmacist, I consider Calcium Citrate the “superior” form of oral calcium compared to the more common Calcium Carbonate, primarily due to its better absorption profile and lower risk of gastrointestinal side effects.

Primary Clinical Uses

  • Osteoporosis Management: A mainstay therapy to increase bone mineral density in postmenopausal women and elderly men to prevent fractures.

  • Calcium Deficiency (Hypocalcaemia): Used to treat or prevent low blood calcium levels in people who do not get enough calcium from their diets.

  • Osteomalacia & Rickets: Essential for the mineralization of the bone matrix in adults (osteomalacia) and children (rickets).

  • Pregnancy & Lactation: Often prescribed to meet the increased physiological demand for calcium, ensuring fetal skeletal development without depleting maternal bone stores.

  • Hypoparathyroidism: Used as a chronic supplement to maintain calcium balance when parathyroid hormone levels are insufficient.

The “Citrate” Advantage: Mechanism of Action

Superior Absorption: Unlike Calcium Carbonate, Calcium Citrate does not require stomach acid for dissolution. This makes it the ideal choice for patients with achlorhydria (low stomach acid), those on PPIs (like Omeprazole), or the elderly.

Vitamin D3 Synergy: Cholecalciferol (D3) acts as a hormone precursor that increases the efficiency of intestinal calcium absorption by upregulating calcium transport proteins. Without D3, only about 10-15% of dietary calcium is absorbed.

Lower Stone Risk: Calcium Citrate may actually reduce the risk of kidney stones compared to other forms, as citrate is a known inhibitor of calcium oxalate crystallization in the urine.

The Manufacturer’s Perspective: Formulation & Export

From a manufacturing and global trade standpoint, this combination is a high-value nutraceutical/pharmaceutical crossover:

  • Tablet Size & Palatability: Calcium Citrate is a bulky molecule. To ensure patient compliance, we focus on film-coated, “easy-swallow” shapes or chewable formats with advanced taste-masking.

  • Vitamin D3 Stability: Vitamin D3 is highly sensitive to light and oxygen. As a WHO-GMP manufacturer, we use stabilized “beadlet” technology for the D3 component and Alu-Alu blister packaging to ensure potency throughout the shelf life.

  • Market Positioning: This is a preferred product for B2B distributors catering to high-end pharmacy chains and orthopedic clinics. It carries a higher margin than basic Calcium Carbonate.

  • Export Logistics: Operating out of Mumbai, we provide CTD Dossiers and stability data tailored for international registration in regions like the CIS, Middle East, and Southeast Asia.

Calcium Carbonate with Vitamin D3 Tablets

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What is calcium carbonate vitamin D3 tablets used for?

In the pharmaceutical industry, the combination of Calcium Carbonate and Vitamin D3 (Cholecalciferol) is a foundational mineral-vitamin supplement. As a pharmacist, I view this formulation as a vital therapeutic tool for bone mineralization and metabolic balance, especially for populations at risk of skeletal degradation.

Primary Clinical Uses

  • Osteoporosis Management: A first-line adjunctive therapy used to increase bone mineral density and reduce the risk of fractures in elderly patients and postmenopausal women.

  • Hypocalcemia: Indicated for the treatment and prevention of low blood calcium levels in patients who do not get enough calcium from their diets.

  • Osteomalacia & Rickets: Used to correct softening of the bones caused by Vitamin D deficiency or impaired calcium absorption.

  • Renal Osteodystrophy: Used as a phosphate binder in patients with chronic renal failure to manage secondary hyperparathyroidism, though this requires strict medical supervision.

Mechanism of Action

This combination is designed for maximum bioavailability:

Calcium Carbonate: Contains a high concentration of elemental calcium (approximately 40%). It serves as a substrate for bone formation and is essential for nerve transmission, muscle contraction, and blood coagulation.

Vitamin D3 (Cholecalciferol): Acts as a hormone precursor that facilitates the active absorption of calcium from the small intestine. Without adequate Vitamin D3, the body cannot absorb calcium efficiently, regardless of how much is ingested.

The Manufacturer’s Perspective: Formulation & Export

From a manufacturing standpoint, producing a high-quality Calcium + D3 tablet involves overcoming specific stability and palatability challenges:

  • Elemental Calcium Loading: We often formulate these as 500 mg or 1000 mg tablets. Achieving a high load of Calcium Carbonate while maintaining a manageable tablet size for the patient is a key engineering goal.

  • Vitamin D3 Stability: Vitamin D3 is highly sensitive to light and oxygen. As a WHO-GMP manufacturer, we utilize micro-encapsulated Vitamin D3 to ensure it remains stable and potent throughout the product’s shelf life.

  • Chewable vs. Film-Coated: To improve patient compliance, we offer chewable tablets with advanced taste-masking (like orange or mint) to hide the “chalky” texture of calcium, as well as film-coated versions for those who prefer swallowing.

  • Global Export Logistics: These are high-volume OTC essentials. Our Mumbai-based facility provides Alu-Alu or HDPE bottle packaging to protect the integrity of the Cholecalciferol, especially for export to African and Southeast Asian markets where high humidity is common.

Calcium Carbonate with Vitamin D3 Tablets

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What is Bromocriptine mesylate used for?

In the pharmaceutical industry, Bromocriptine Mesylate tablets (commonly manufactured in 0.8 mg, 2.5 mg, and 5 mg strengths) are a potent ergot derivative that acts as a dopamine D2 receptor agonist. As a pharmacist, I view Bromocriptine as a versatile endocrine and neurological regulator that bridges the gap between hormone management and movement disorders.

Primary Clinical Uses

  • Hyperprolactinemia-Associated Disorders: The primary treatment for conditions caused by high prolactin, including amenorrhea (loss of menstrual cycle), galactorrhea (unexplained milk production), and infertility.

  • Prolactinomas: Used to shrink prolactin-secreting pituitary adenomas (benign tumors).

  • Acromegaly: Indicated to reduce elevated Growth Hormone (GH) levels in patients who have not responded sufficiently to surgery or radiation.

  • Parkinson’s Disease: Used as an adjunct to Levodopa/Carbidopa to manage the signs and symptoms of idiopathic or postencephalitic Parkinson’s.

  • Type 2 Diabetes Mellitus: A specific quick-release formulation (Cycloset) is used to improve glycemic control by modulating circadian rhythm-mediated glucose metabolism.

Mechanism of Action

Bromocriptine acts by directly stimulating postsynaptic dopamine D2 receptors in the brain.

In the Pituitary Gland: It mimics the action of dopamine (the “prolactin-inhibiting factor”), thereby suppressing the synthesis and secretion of prolactin from the anterior pituitary.

In the Corpus Striatum: For Parkinson’s, it compensates for the lack of endogenous dopamine, helping to restore the balance required for smooth muscle movement and coordination.

The Manufacturer’s Perspective: Formulation & Export

From a manufacturing and global trade standpoint, Bromocriptine is a high-precision, specialty molecule:

  • API Sensitivity: Bromocriptine Mesylate is highly sensitive to light and oxidation. As a WHO-GMP manufacturer, we utilize specialized light-resistant coating and amber-colored packaging to ensure the API does not degrade during its shelf life.

  • Micronization: Given the low dosage (2.5 mg), we employ micronization techniques to ensure uniform particle size, which is critical for consistent dissolution and absorption.

  • Global Export Profile: This is a high-value niche product for B2B distributors catering to endocrinology and neurology clinics. Our Mumbai facility is equipped to provide the CTD/eCTD Dossiers required for registration in regulated and semi-regulated markets.

  • Stability for Export: We provide stability data for Zone IVb conditions, ensuring that the product remains potent even when exported to hot and humid regions in Africa and Southeast Asia.

 

Bromocriptin Tablets

 

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What is Bisoprolol Fumarate used for?

In the pharmaceutical industry, Bisoprolol Fumarate tablets (typically 2.5 mg, 5 mg, and 10 mg) are a highly cardioselective beta-1 adrenergic receptor blocker. As a pharmacist, I view Bisoprolol as a vital therapeutic agent because its high selectivity for the heart minimizes side effects on the lungs (bronchospasm), making it a safer option than older, non-selective beta-blockers.

Primary Clinical Uses

  • Hypertension (High Blood Pressure): It lowers blood pressure by reducing the force of the heart’s contraction and slowing the heart rate.

  • Stable Chronic Heart Failure: Usually prescribed as an add-on therapy to ACE inhibitors and diuretics to improve long-term cardiac survival and reduce hospitalizations.

  • Angina Pectoris: Used for the long-term management of chest pain by reducing the heart’s oxygen demand during physical exertion.

  • Tachyarrhythmias: Helps control irregular or abnormally fast heartbeats by stabilizing the heart’s electrical conduction.

Mechanism of Action

Bisoprolol competitively blocks $\beta_1$-adrenergic receptors, which are predominantly located in the heart muscle and the juxtaglomerular cells of the kidney.

Cardiac Effect: It inhibits the stimulatory effects of adrenaline (epinephrine), leading to a decrease in heart rate (negative chronotropic effect) and a decrease in the force of contraction (negative inotropic effect).

Renal Effect: It blocks the release of renin, thereby inhibiting the Renin-Angiotensin-Aldosterone System (RAAS), which leads to vasodilation and reduced fluid retention.

The Manufacturer’s Perspective: Formulation & Export

From a manufacturing and global trade standpoint, Bisoprolol Fumarate is a precision molecule that fits perfectly into an export-oriented portfolio:

  • Dose Uniformity: Because Bisoprolol is effective at very low doses (as low as 1.25 mg or 2.5 mg), we utilize validated micronization and blending techniques to ensure absolute content uniformity in every tablet.

  • Bilayer & Combination FDCs: We often develop Fixed-Dose Combinations (FDCs) of Bisoprolol + Hydrochlorothiazide or Bisoprolol + Amlodipine to enhance patient compliance in resistant hypertension cases.

  • Stability for Export: Bisoprolol is a stable API, but as a WHO-GMP manufacturer, we prioritize Alu-Alu blister packaging to ensure its 36-month shelf life remains intact during transit to Zone IVb regions (hot and humid) like Africa and Southeast Asia.

  • Regulatory Documentation: Our Mumbai-based hub supports international B2B partners by providing full CTD/eCTD Dossiers and comparative dissolution studies against the innovator (Concor/Zebeta) for rapid registration.

Bisoprolol Tablets

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What is Bisacodyl tablet used for?

In the pharmaceutical industry, Bisacodyl tablets (standardized at 5 mg) are a potent stimulant laxative of the diphenylmethane derivative group. As a pharmacist, I view Bisacodyl as a highly reliable, predictable medication for managing bowel motility, particularly when rapid or scheduled evacuation is clinically required.

Primary Clinical Uses

  • Acute Constipation: Provides short-term relief for occasional constipation by stimulating bowel movements.

  • Bowel Clearance for Medical Procedures: Used as a primary “bowel prep” agent before colonoscopies, X-rays, or abdominal surgeries to ensure the intestines are clear.

  • Neurogenic Bowel Dysfunction: Managed in patients with spinal cord injuries or other neurological conditions to maintain regular bowel habits.

  • Post-Operative Recovery: Occasionally used to restore bowel function after surgery (once bowel sounds return).

Mechanism of Action

Bisacodyl is a prodrug. When taken orally, it is hydrolyzed by intestinal enzymes into its active metabolite (BHPM). It works through two main pathways:

Direct Stimulation: It acts directly on the sensory nerve endings in the colonic mucosa to stimulate peristalsis (the wave-like muscle contractions of the intestines).

Fluid Accumulation: It increases the secretion of water and electrolytes into the intestinal lumen, softening the stool and increasing the volume, which further triggers the urge to evacuate.

Technical Note: Because the tablets are enteric-coated to protect the stomach from irritation and ensure the drug reaches the colon, they must be swallowed whole. Taking them with antacids or milk can break the coating prematurely, leading to gastric distress.

The Manufacturer’s Perspective: Formulation & Export

From a manufacturing and global trade standpoint, Bisacodyl is a high-volume OTC (Over-the-Counter) staple:

  • Enteric Coating Technology: As a WHO-GMP manufacturer, our primary focus is the precision of the enteric coating (pH-sensitive). We ensure the tablet does not dissolve in the stomach’s acidic environment ($pH < 5.5$) but disintegrates rapidly in the neutral environment of the small intestine.

  • Dose Uniformity: With a 5 mg dose, we utilize validated granulation and compression techniques to ensure consistent efficacy across every batch.

  • Global Export Profile: Bisacodyl is a high-demand item for B2B distributors and pharmacy chains worldwide. Its stability makes it ideal for export in PVC/PVDC or Alu-Alu blister packs to the Middle East, Africa, and Southeast Asia.

  • Regulatory Support: We provide comprehensive CTD Dossiers and stability data for Zone IVb to support our international partners in rapid registration and market entry.

Bisacodyl Tablets

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What is Biperiden Hydrochloride used for?

In the pharmaceutical industry, Biperiden Hydrochloride tablets (typically 2 mg) are a potent synthetic anticholinergic agent used primarily for its effects on the central nervous system. As a pharmacist, I characterize Biperiden as a critical “corrective” medication, essential for restoring the balance between the dopaminergic and cholinergic systems in the brain.

Primary Clinical Uses

  • Parkinson’s Disease: Used as adjunctive therapy in all forms of Parkinsonism (postencephalitic, arteriosclerotic, or idiopathic). it is particularly effective in reducing muscle rigidity and tremors.

  • Extrapyramidal Symptoms (EPS): This is its most frequent modern application. It is used to control drug-induced movement disorders caused by antipsychotic medications (neuroleptics), such as acute dystonia, akathisia, and secondary Parkinsonism.

  • Nicotine Poisoning: Occasionally utilized in specific clinical settings as an antidote for nicotine poisoning due to its antagonistic effects on nicotinic receptors.

Mechanism of Action

Biperiden is a selective central nervous system anticholinergic. It works by competitively antagonizing acetylcholine at the muscarinic receptors. In the striatum of the brain, Parkinsonian symptoms occur when there is an imbalance—specifically, too little dopamine and too much cholinergic activity. Biperiden acts to dampen that excessive cholinergic signaling, thereby reducing involuntary muscle movements and stiffness.

The Manufacturer’s Perspective: Formulation & Export

From a manufacturing and global trade standpoint, Biperiden is a specialized CNS (Central Nervous System) molecule that fits into “niche” psychiatric and neurological portfolios:

  • Potency and Precision: Because Biperiden is highly potent at a low dose (2 mg), our manufacturing process involves high-shear granulation to ensure absolute content uniformity across every tablet in the batch.

  • Stability & Shelf Life: Biperiden Hydrochloride is generally stable, but we utilize Alu-PVC or Alu-Alu packaging to ensure the product maintains its chemical integrity when exported to varied climates, specifically targeting the CIS, Middle East, and Southeast Asian markets.

  • Global Demand: While not as high-volume as a generic antibiotic, Biperiden is a “mandatory” stock item for psychiatric hospitals and B2B distributors who handle neuroleptic medications, as it is the primary rescue medication for EPS.

  • Regulatory Support: As a WHO-GMP facility, we provide the necessary CTD Dossiers and stability data to facilitate the registration of this CNS agent in international markets, ensuring a reliable supply for specialized healthcare sectors.

Biperiden Tablets

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What is Trihexyphenidyl Hydrochloride Tablets used for?

In the pharmaceutical industry, Trihexyphenidyl Hydrochloride tablets (commonly manufactured in 2 mg and 5 mg strengths) are a potent antispasmodic and anticholinergic agent. As a pharmacist, I view Trihexyphenidyl as an essential corrective medication, primarily used to restore the balance between the dopamine and acetylcholine neurotransmitter systems in the brain.

Primary Clinical Uses

  • Parkinson’s Disease: Indicated as an adjunctive treatment for all forms of parkinsonism (postencephalitic, arteriosclerotic, and idiopathic). It is particularly effective in reducing muscular rigidity and tremors.

  • Extrapyramidal Symptoms (EPS): Frequently co-prescribed with antipsychotic medications (like Haloperidol or Chlorpromazine) to control drug-induced movement disorders, such as akathisia, dystonia, and pseudo-parkinsonism.

  • Control of Sialorrhea: Used off-label to manage excessive drooling in patients with neurological conditions due to its potent drying (antisecretory) effects.

Mechanism of Action

Trihexyphenidyl acts as a competitive antagonist at muscarinic acetylcholine receptors ($M_1$ subtype) in the central nervous system. In conditions like Parkinson’s, there is a functional deficiency of dopamine, which leads to a relative overactivity of acetylcholine. By blocking these cholinergic pathways in the striatum, Trihexyphenidyl helps suppress the excitatory signals that cause tremors and muscle stiffness.

The Manufacturer’s Perspective: Formulation & Export

From a manufacturing and global trade standpoint, Trihexyphenidyl is a high-precision CNS (Central Nervous System) drug that requires strict quality control:

  • Dose Uniformity: Because this molecule is highly potent at low doses (2 mg), our manufacturing process utilizes validated blending and granulation techniques to ensure absolute content uniformity in every single tablet.

  • Stability & Shelf-Life: Trihexyphenidyl HCl is relatively stable, but as a WHO-GMP manufacturer, we utilize moisture-resistant packaging (PVC/PVDC or Alu-Alu) to maintain integrity during export to Zone IVb regions (Africa, SE Asia).

  • B2B & Niche Demand: While not a “mass-market” drug like Paracetamol, it is a high-value niche product for psychiatric hospitals and neurology clinics. It is a staple for B2B distributors catering to mental health facilities globally.

  • Regulatory Documentation: We provide full CTD Dossiers and stability data to support our international partners, ensuring the product meets international pharmacopeial standards (BP/USP/IP).

Trihexyphenidyl Hydrochloride Tablets

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What is the use of Azithromycin dispersible tablets?

In the pharmaceutical industry, Azithromycin Dispersible Tablets (typically 100 mg or 250 mg) are a specialized pediatric formulation of the macrolide antibiotic class. As a pharmacist, I view the dispersible format as a critical advancement in “patient-centric” medicine—ensuring that children receive the precise, potent dose of a broad-spectrum antibiotic without the struggle of swallowing large pills or the stability issues often found in liquid suspensions.

Primary Clinical Uses

  • Upper Respiratory Tract Infections (URTI): Highly effective for tonsillitis, pharyngitis, and acute sinusitis.

  • Lower Respiratory Tract Infections (LRTI): A first-line treatment for community-acquired pneumonia and acute bacterial exacerbations of bronchitis.

  • Acute Otitis Media: The primary choice for middle ear infections in children due to its high tissue penetration.

  • Skin and Soft Tissue Infections: Used for uncomplicated infections caused by Staphylococcus aureus or Streptococcus pyogenes.

Mechanism of Action

Azithromycin works by binding to the 50S ribosomal subunit of susceptible microorganisms. This action interferes with microbial protein synthesis by inhibiting the transpeptidation/translocation step.

What makes Azithromycin unique from a pharmacokinetic standpoint is its extensive tissue distribution. It concentrates within lysosomes and white blood cells (phagocytes), which then “transport” the drug directly to the site of infection. This results in high local concentrations and allows for a convenient once-daily dosing schedule.

The Manufacturer’s Perspective: Formulation & Export

From a manufacturing and global trade standpoint, the dispersible tablet is a high-tech solution for global health:

  • Instant Disintegration: As a WHO-GMP standard, these tablets are formulated to disintegrate in less than 60 seconds in a teaspoon of water, forming a smooth suspension that is easy for infants and children to swallow.

  • Taste-Masking Excellence: Azithromycin API is notoriously bitter. Our formulation involves advanced taste-masking technology and fruit flavors (like strawberry or mango) to ensure pediatric compliance and prevent “spit-ups.”

  • Stability in Transit: Unlike liquid syrups which require bulky glass bottles and have shorter shelf lives once reconstituted, dispersible tablets are lightweight and highly stable. We utilize Alu-Alu blister packaging to protect the API from moisture and light, making it ideal for export to Zone IVb climates.

  • Global Market Demand: These tablets are essential for B2B distributors and international NGO tenders (like UNICEF) catering to pediatric health in Africa, Southeast Asia, and the Middle East.

Azithromycin Dispersible Tablet

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What is Azatioprine used to treat?

In the pharmaceutical industry, Azathioprine tablets (commonly 50 mg) are classified as a potent immunosuppressant and a prodrug of 6-mercaptopurine. As a pharmacist, I view Azathioprine as a critical “steroid-sparing” agent, allowing clinicians to reduce long-term corticosteroid use while maintaining control over the immune system.

Primary Clinical Uses

  • Organ Transplant Rejection: Used as a mainstay adjunctive therapy to prevent the rejection of kidney, heart, and liver transplants, typically in combination with other immunosuppressants.

  • Rheumatoid Arthritis (RA): Indicated for patients with severe, active RA who have not responded to conventional first-line Disease-Modifying Anti-Rheumatic Drugs (DMARDs).

  • Inflammatory Bowel Disease (IBD): Widely used to maintain remission in patients with Crohn’s Disease and Ulcerative Colitis.

  • Autoimmune Disorders: Effective in treating Systemic Lupus Erythematosus (SLE), autoimmune hepatitis, and Myasthenia Gravis.

Mechanism of Action

Azathioprine is a purine antimetabolite. Once ingested, it is rapidly converted into 6-mercaptopurine (6-MP). It acts by interfering with DNA and RNA synthesis within rapidly dividing cells, particularly T-lymphocytes and B-lymphocytes. By inhibiting the proliferation of these immune cells, Azathioprine suppresses the body’s autoimmune attack or the rejection response against a donor organ.

Technical Note: The metabolism of Azathioprine depends on the enzyme TPMT (Thiopurine Methyltransferase). As a pharmacist, I always emphasize that patients should ideally be screened for TPMT activity before starting therapy to avoid severe bone marrow toxicity.

The Manufacturer’s Perspective: Formulation & Export

From a manufacturing and global trade standpoint, Azathioprine is a high-sensitivity molecule requiring rigorous quality standards:

  • Cytotoxic Handling: Azathioprine is a potent substance. In our manufacturing processes, we adhere to strict containment protocols and WHO-GMP standards to prevent cross-contamination and ensure worker safety.

  • Stability & Coating: The tablets are typically film-coated to protect the active ingredient from light and to prevent dust exposure during handling. We ensure the coating provides a robust barrier for long-term stability in export conditions.

  • Global Export Niche: Azathioprine is a vital product for B2B marketplaces and hospital supply chains catering to oncology and transplant centers in the CIS, Middle East, and Africa.

  • Documentation: We provide full CTD/eCTD Dossiers, including stability data for Zone IVb, to facilitate registration in international markets where chronic disease management is expanding.

Azathioprine Tablets

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What are Atorvastatin Tablets used for?

In the pharmaceutical industry, Atorvastatin Calcium tablets (commonly manufactured in 10 mg, 20 mg, 40 mg, and 80 mg strengths) are the premier HMG-CoA reductase inhibitors, more commonly known as “statins.” As a pharmacist, I view Atorvastatin as a cornerstone of lipid-lowering therapy due to its superior ability to reduce LDL cholesterol and provide significant pleiotropic benefits for cardiovascular stability.

Primary Clinical Uses

  • Hypercholesterolemia: Indicated as an adjunct to diet to reduce elevated total cholesterol, LDL-C (“bad” cholesterol), and triglycerides, while increasing HDL-C (“good” cholesterol).

  • Prevention of Cardiovascular Disease: Used to reduce the risk of myocardial infarction (heart attack), stroke, and revascularization procedures in patients with or without clinically evident coronary heart disease.

  • Dysbetalipoproteinemia: Effective for patients with primary dysbetalipoproteinemia who do not respond adequately to diet.

  • Secondary Prevention: Indicated for patients with established coronary heart disease to reduce the risk of non-fatal myocardial infarction and fatal/non-fatal stroke.

Mechanism of Action

Atorvastatin works by selectively and competitively inhibiting HMG-CoA reductase, the rate-limiting enzyme that converts 3-hydroxy-3-methylglutaryl-coenzyme A to mevalonate, a precursor of sterols, including cholesterol. By reducing hepatic cholesterol synthesis, it triggers an up-regulation of LDL receptors on the surface of liver cells, which enhances the uptake and catabolism of LDL from the blood.

The Manufacturer’s Perspective: Formulation & Export

From a manufacturing and global trade standpoint, Atorvastatin is a high-demand, technically demanding molecule:

  • Amorphous vs. Crystalline Form: As a WHO-GMP manufacturer, we carefully control the physical form of the API. While the crystalline form is often preferred for its stability, the formulation must be optimized to ensure high bioavailability and consistent dissolution rates.

  • Stability & Oxidation: Atorvastatin is sensitive to heat, light, and moisture. We utilize Alu-Alu blister packaging and include antioxidants in the formulation to ensure a stable 24-month shelf life, especially for export to Zone IVb (hot and humid) regions.

  • Dose Versatility: We manufacture the full range of strengths (10 mg to 80 mg) to allow for the “high-intensity statin therapy” required for high-risk cardiac patients.

  • Global Market Access: Atorvastatin is one of the most exported chronic care medications. Our Mumbai-based hub provides full CTD/eCTD Dossier support for registration in international markets across Africa, the CIS, and Southeast Asia.

Atorvastatin Tablets

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