FDA NDC Directory · JSON-LD · Markdown

NEVIRAPINE

NDC 42571-131 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA203080
Dosage form / routeTABLET · ORAL
Active ingredientsNEVIRAPINE (200 mg/1)
Marketing started20120522
Package count2

External sources

Source: openFDA. Public-domain (CC0).