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Raltegravir

NDC 70748-327 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217990
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsRALTEGRAVIR POTASSIUM (600 mg/1)
Marketing started20261014
Package count1

External sources

Source: openFDA. Public-domain (CC0).