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Azithromycin & Cefixime tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Film-Coated Tablet, packed in high-barrier Alu-Alu blister strips to prevent the degradation of the moisture-sensitive API.
Active Ingredient Strength Primary Clinical Function Cefixime (as Trihydrate) USP/BP 200 mg The Gram-Negative Specialist: Targets the cell walls of stubborn bacteria, highly effective in Typhoid and Bronchitis. Azithromycin (as Dihydrate) USP/BP 250 mg / 500 mg The Tissue-Penetrating Anchor: Provides prolonged activity in the lungs and soft tissues to eliminate intracellular pathogens. Excipients Proprietary Matrix Dual-Release System: Engineered to ensure synchronized absorption of both antibiotics despite their different chemical solubilities. Azithromycin Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The coating is essential to mask the extremely bitter taste and facilitate swallowing.
Active Ingredient Strength (Standard) Standard Regimen Primary Role Azithromycin Dihydrate USP/BP 250 mg 6 Tablets (3-5 Days) Step-down Therapy / Pediatric Azithromycin Dihydrate USP/BP 500 mg 3 Tablets (3 Days) Respiratory Infections / Typhoid Azithromycin Dihydrate USP/BP 1000 mg (1 g) 1 Tablet (Single Dose) STI (Chlamydia / Gonorrhea) Excipients Q.S. Pregelatinized Starch / HPMC Disintegration / Coating Cefepime & Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 2:1.
Strength Variant Cefepime Content Sulbactam Content Ratio 1.5 g Vial 1000 mg (1 g) 500 mg (Sodium) 2:1 (Standard) Excipients L-Arginine Buffer / Stabilizer – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefepime & Tazobactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 8:1.
Strength Variant Cefepime Content Tazobactam Content Ratio 1.125 g Vial 1000 mg (1 g) 125 mg (Sodium) 8:1 (Standard) Excipients L-Arginine Buffer / Stabilizer – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefepime Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It contains L-Arginine as a buffering agent (instead of sodium salts).
Active Ingredient Strength Therapeutic Role Cefepime Hydrochloride USP/BP Equivalent to 1000 mg (1 g) Cefepime Severe Infection / Sepsis Cefepime Hydrochloride USP/BP Equivalent to 500 mg Cefepime Pediatric / Moderate Infection Buffer L-Arginine pH Stabilizer (Approx 725 mg per g) *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefoperazone & Sulbactam 2Gm Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in 20ml glass vials.
Active Ingredient Strength Function Cefoperazone Sodium USP/BP 1000 mg (1 g) Anti-Pseudomonal Cephalosporin Sulbactam Sodium USP/BP 1000 mg (1 g) Beta-Lactamase Inhibitor Ratio 1 : 1 High Sulbactam Load *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with 10ml Water for Injection (WFI).
Cefoperazone & Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 1:1.
Strength Variant Cefoperazone Content Sulbactam Content Ratio 1.5 g Vial 500 mg (Sodium) 500 mg (Sodium) 1:1 (Standard) 3.0 g Vial 1000 mg (1 g) 1000 mg (1 g) 1:1 (High Dose) Excipients None (Sterile Blend) – – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefoperazone & Tazobactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 8:1.
Strength Variant Cefoperazone Content Tazobactam Content Ratio 1.125 g Vial 1000 mg (1 g) 125 mg (Sodium) 8:1 (Standard) Excipients None (Sterile Blend) – – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
1.125 g Vial 1000 mg (1 g) 125 mg (Sodium) 8:1 (Standard) Excipients None (Sterile Blend) – – Cefoperazone Sodium Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It contains approximately 34 mg (1.5 mEq) of sodium per gram.
Active Ingredient Strength (Standard) Therapeutic Role Cefoperazone Sodium USP/BP Equivalent to 1000 mg (1 g) Cefoperazone Adult Surgical / Biliary Dose Excipients None (Pure Sterile Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefotaxime Sodium Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The sodium content is lower than many other cephalosporins (approx 2.2 mmol/g).
Active Ingredient Strength Primary Patient Cefotaxime Sodium USP/BP Equivalent to 1000 mg (1 g) Adults (Meningitis/Sepsis) Cefotaxime Sodium USP/BP Equivalent to 500 mg Pediatrics Cefotaxime Sodium USP/BP Equivalent to 250 mg Neonates / Infants Excipients None (Pure Sterile Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefpirome & Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 2:1.
Strength Variant Cefpirome Content (as Sulfate) Sulbactam Content (as Sodium) Ratio 1.5 g Vial 1000 mg (1 g) 500 mg 2:1 (Standard) Excipients Sodium Carbonate Buffer – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefpirome Sulfate Injection
FreeCefpirome sulfate injection is a fourth-generation cephalosporin antibiotic typically supplied as a sterile dry powder for intravenous (IV) or intramuscular (IM) administration
Ceftazidime & Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is either 2:1 or 1:1 depending on the market requirement.
Strength Variant Ceftazidime Content Sulbactam Content Ratio 1.5 g Vial 1000 mg (1 g) 500 mg (Sodium) 2:1 (Standard) 2.25 g Vial 1125 mg 1125 mg 1:1 (High Potency) Excipients Sodium Carbonate Buffer – *Pack Sizes: Tray of 1 Vial or Box of 1/10 Vials with Water for Injection (WFI).
Ceftazidime & Tazobactam Injection
FreeCeftazidime and tazobactam injection is a combination antibiotic used primarily in hospital settings for serious, multi-drug resistant bacterial infections. It is typically available as a sterile dry powder for reconstitution.
Product Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 8:1.
Strength Variant Ceftazidime Content Tazobactam Content Target Patient 1.125 g Vial 1000 mg (1 g) 125 mg (Sodium) Standard Adult Dose 281.25 mg Vial 250 mg 31.25 mg Pediatric Dose Excipients Sodium Carbonate Buffer Solubilizer Ceftazidime Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It contains Sodium Carbonate as a solubilizer.
Active Ingredient Strength Primary Patient Ceftazidime Pentahydrate USP/BP Equivalent to 1000 mg (1 g) Adults (Standard Dose) Ceftazidime Pentahydrate USP/BP Equivalent to 250 mg Pediatrics / Neonates Excipients Sodium Carbonate Gas-Releasing Buffer *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ceftriaxone & Sulbactam injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 2:1.
Strength Variant Ceftriaxone Content Sulbactam Content Target Patient 1.5 g Vial 1000 mg (1 g) 500 mg (Sodium) Adult Standard Dose 750 mg Vial 500 mg 250 mg Pediatric / Moderate Dose 375 mg Vial 250 mg 125 mg Infant / Neonate Dose Ratio 2 : 1 – Optimal Synergy *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ceftriaxone & Tazobactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 8:1.
Strength Variant Ceftriaxone Content Tazobactam Content Ratio 1.125 g Vial 1000 mg (1 g) 125 mg (Sodium) 8:1 (Standard) 562.5 mg Vial 500 mg 62.5 mg Pediatric Excipients None (Sterile Blend) – – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ceftriaxone 1gm Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials.
Active Ingredient Strength Standard Use Ceftriaxone Sodium USP/BP Equivalent to 1000 mg (1 g) Ceftriaxone Adult Standard Dose Sodium Content Approx 83 mg (3.6 mEq) Per 1g Vial *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ceftriaxone 500mg Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials.
Active Ingredient Strength Target Use Ceftriaxone Sodium USP/BP Equivalent to 500 mg Ceftriaxone Pediatrics / IM Gonorrhea Sodium Content Approx 41.5 mg (1.8 mEq) Low Sodium Load *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefuroxime & Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 2:1.
Strength Variant Cefuroxime Content Sulbactam Content Primary Use 1.5 g Vial 1000 mg (1 g) 500 mg (Sodium) Adult Therapy / Surgery 1.125 g Vial 750 mg 375 mg Moderate Infection 375 mg Vial 250 mg 125 mg Pediatrics *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefuroxime Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials.
Active Ingredient Strength Primary Use Cefuroxime Sodium USP/BP Equivalent to 750 mg Cefuroxime Standard Adult Dose Cefuroxime Sodium USP/BP Equivalent to 1500 mg (1.5 g) Severe Infections / Surgery Excipients None (Pure Sterile Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cephalothin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It contains approximately 2.8 mEq (64 mg) of Sodium per gram.
Active Ingredient Strength Therapeutic Role Cephalothin Sodium USP/BP Equivalent to 1000 mg (1 g) Cephalothin Surgical Prophylaxis / Skin Infection Excipients Sodium Bicarbonate Buffer / pH Adjuster *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Clarithromycin Tablets
FreeClarithromycin Tablets USP 500 mg
Each Filmcoated tablet contains :
Clarithromycin USP 500 mgUsage: – Chest infections
Category: – Antibiotic drugs
Therapeutic category: – Antibiotic
Co -Trimoxazole Tablets Tablet
FreeCo- Trimoxazole Tablets IP
Trimethoprime & Sulphamethoxazole Tablets IP
Each Uncoated tablet contains :
Trimethoprime IP 20 mg
Sulphamethoxazole IP 100 mgTrimethoprim & sulphamethoxazole tablets IP Co -trimoxazole Tablets IP
Each film coated tablets : Excipients q.s
Trimethoprim IP 80 mg
Sulphamethoxazole IP 400 mgTrimethoprim & sulphamethoxazole tablets IP
Each film coated tablets :
Trimethoprim IP 160 mg
Sulphamethoxazole IP 800 mgCo – Trimoxazole Tablets BP
Trimethoprim & Sulphamethoxazole Tablets BP
Each Uncoated Tablet contains :
Trimethoprim BP 80 mg
Sulfamethoxazole BP 400 mgTACOT – DS
Trimethoprim & Sulphamethoxazole Tablets BP
Each Uncoated tablet contains :
Trimethoprim BP 160 mg
Sulphamethoxazole BP 800 mgUsage: – Traveler’s diarrhea
Category: – Antibiotic drugs
Therapeutic category: – Antibiotic
Doripenem Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Primary Use Doripenem Monohydrate USP/BP Equivalent to 500 mg Doripenem Standard Adult Dose Doripenem Monohydrate USP/BP Equivalent to 250 mg Renal Impairment Excipients None (Pure Sterile Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials.
Imipenem & Cilastatin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Buffered Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Role Imipenem USP/BP 500 mg Antibiotic (Carbapenem) Cilastatin Sodium USP/BP Equivalent to 500 mg Cilastatin DHP-I Inhibitor Buffer Sodium Bicarbonate pH Stabilizer *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials.
Levofloxacin Tablets
FreeProduct Composition & Available Portfolio
We manufacture Levofloxacin across the complete, internationally standardized therapeutic spectrum to accommodate customized tissue-saturation requirements and specific treatment durations.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Levofloxacin Hemiandrous / Monohydrate USP / BP / IP 250 mg Oral Solid Film-Coated Tablet Uncomplicated Infections: For standard low-dose management of uncomplicated urinary tract infections (UTIs) and acute bacterial sinusitis. Levofloxacin Hemiandrous / Monohydrate USP / BP / IP 500 mg Oral Solid Film-Coated Tablet The Core Commercial Volume: First-line international standard for community-acquired pneumonia (CAP), skin structures, and acute pyelonephritis. Levofloxacin Hemiandrous / Monohydrate USP / BP / IP 750 mg Oral High-Potency Solid Tablet Intensive High-Dose Short-Course: Calibrated for nosocomial pneumonia, complicated skin infections, and advanced multi-drug resistant (MDR) regimens. Mefloquine Tablet
FreeProduct Composition & Configuration
We supply Mefloquine Hydrochloride in the internationally standardized strength calibrated for both adult therapeutic clearance and weekly travel prophylaxis.
Active Ingredient Monograph Calibrated Strength Formulation Delivery Matrix Primary Clinical Application Mefloquine Hydrochloride IP / BP / USP 250 mg
(Equivalent to 228 mg Mefloquine Base)
Oral Solid Uncoated Tablet (Cross-scored for exact pediatric dividing) Dual-Mode Antimalarial: High-dose 3-day treatment for active clearance, or low-dose once-weekly regimen for traveler chemoprophylaxis. Excipients Pharma Grade Microcrystalline Cellulose, Lactose, Magnesium Stearate The Disintegration Core: Engineered for uniform mechanical compression and rapid disintegration. Meropenem & Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Role Meropenem USP/BP 1000 mg (1 g) Broad-Spectrum Carbapenem Sulbactam Sodium USP/BP Equivalent to 500 mg Beta-Lactamase Inhibitor Total Strength 1.5 g (1500 mg) Per Single Dose Vial *Pack Sizes: Single Vial with or without Sterile Water for Injection.
Meropenem Injection
FreeMeropenem injection (brand name Keppra) is a broad-spectrum carbapenem antibiotic supplied as a sterile white to pale yellow powder for reconstitution. It is used to treat severe bacterial infections
Nalidixic Tablet
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets. The formulation is engineered for rapid disintegration to ensure the active ingredient is quickly processed for renal excretion.
Active Ingredient Strength (Standard) Therapeutic Role Nalidixic Acid BP/USP 500 mg Quinolone Antibacterial Excipients Q.S. Maize Starch / Gelatin Binder & Disintegrant Coating (Optional) Q.S. HPMC / Titanium Dioxide Film Coating Nystatin Tablet
FreeProduct Composition & Configuration
We supply this product in the internationally recognized standard therapeutic strength optimized for uniform, localized mucosal distribution.
Active Ingredient Strength (per Tablet) Formulation Delivery System Primary Clinical Function Nystatin IP / BP / USP 100,000 IU Non-Effervescent Local Insert: Designed for slow physical disintegration within vaginal mucosal fluids. The Polyene Fungicide: Eradicates superficial Candida strains locally. Excipients Pharma Grade Modified lactose, starch, and lubricating binding agents. The Comfort Base: Ensures non-irritating, smooth insertion profiles. Rifampicin & Isoniazid Tablets
FreeProduct Composition & Standard Compendial Configurations
We supply this FDC in the internationally recognized, World Health Organization (WHO) recommended dosage strengths calibrated to support exact adult and pediatric weight-band categories.
Active Ingredients Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Rifampicin + Isoniazid BP/USP/IP 150 mg + 75 mg Oral Solid Film-Coated Tablet Adult Continuation Phase: Standard international baseline configuration utilized daily for the 4-month consolidation phase of pulmonary tuberculosis. Rifampicin + Isoniazid BP/USP/IP 300 mg + 150 mg Oral High-Mass Film-Coated Tablet High-Weight Adult Maintenance: High-potency format optimized to ensure single-tablet compliance for patients in higher weight bands. Rifampicin + Isoniazid BP/USP/IP 60 mg + 30 mg / 60 mg + 60 mg Oral Solid Soluble / Dispersible Tablet Pediatric Regimen Management: Fruit-flavored, water-soluble dispersible matrices engineered for exact dose compliance in pediatric networks. Rifampicin Isoniazide Pyrizinamide Tablets
FreeRifampicin, Isoniazide and Pyrizinamide Tab (Combi Pack)
(Rifampicin Tablets IP) + (Isoniazide Tablets IP) + (Pyrizinamide Tablets IP)
Each film Coated Tablet Contains :
Rifampicin IP 100 mg
Each coated Tablet Contains :
Isonoazide IP 50 mg
Each coated Tablet contains :
Pyrizinamide IP 250 mgRIP TABLETS
(Rifampicin, Isoniazid And Pyrazinamide Tablets Int.Ph.)
Each Filmcoated Tablet Contains:
Rifampicin BP/Int.Ph. 150 mg
Isoniazid BP/Int.Ph. 75 mg
Pyrazinamide BP/Int.Ph. 400 mgUsage: – treat tuberculosis (TB) infection
Category: – Antibiotic drugs
Therapeutic category: – Antibiotic, Antituberculosis
Rifampicin, Isoniazid, Pyrazinamide & Ethambutol Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (usually Brown or Reddish-Brown). We offer both the “Daily Regimen” and “Intermittent Regimen” strengths.
Active Ingredient Strength (WHO Daily FDC) Therapeutic Role Rifampicin IP/BP/USP 150 mg Sterilizing / Broad Spectrum Isoniazid IP/BP/USP 75 mg Early Bactericidal Pyrazinamide IP/BP/USP 400 mg Intracellular Sterilizing Ethambutol HCl IP/BP/USP 275 mg Resistance Prevention Roxithromycin Tablets
FreeRoxiron-150
(Roxithromycin tablets 150 mg)
Each Film coated tablets contains:
Roxithromycin BP 150 mgUsage: – treats bacterial infections
Category: – Antibiotic drugs
Therapeutic category: – Antibiotic


















