Lamivudine, Zidovudine & Nevirapine Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (often White or Off-White). This FDC is designed for patients who have successfully completed the Nevirapine “lead-in” phase.
Active Ingredient Strength (Standard) Class Lamivudine USP/BP 150 mg NRTI (Cytidine Analog) Zidovudine USP/BP 300 mg NRTI (Thymidine Analog) Nevirapine USP/BP 200 mg NNRTI Excipients Q.S. Microcrystalline Cellulose / Sodium Starch Glycolate Nevirapine Tablet
FreeProduct Composition & Strengths
We supply this antiretroviral therapeutic in the globally accepted standard therapeutic strength optimized for adult combination maintenance therapy.
Active Ingredient Standard Strength Formulation Delivery Matrix Primary Clinical Function Nevirapine Anhydrous IP / BP / USP 200 mg Oral Solid Uncoated Tablet (Scored for flexible pediatric/titration dividing) The NNRTI Anchor: Suppresses viral replication loads when used in combination ARV regimens. Excipients Pharma Grade Lactose, Microcrystalline Cellulose, Sodium Starch Glycolate The Delivery Core: Ensures immediate physical disintegration and release kinetics.
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