FDA NDC Directory · JSON-LD · Markdown

Atazanavir Sulfate

NDC 65862-712 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameAtazanavir
Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA204806
Dosage form / routeCAPSULE · ORAL
Active ingredientsATAZANAVIR SULFATE (200 mg/1)
Marketing started20180625
Package count4

External sources

Source: openFDA. Public-domain (CC0).