FDA NDC Directory · JSON-LD · Markdown

Nevirapine

NDC 33342-004 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA090688
Dosage form / routeTABLET · ORAL
Active ingredientsNEVIRAPINE (200 mg/1)
Marketing started20190128
Package count1

External sources

Source: openFDA. Public-domain (CC0).