FDA NDC Directory · JSON-LD · Markdown

emtricitabine

NDC 69097-642 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerCipla USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091168
Dosage form / routeCAPSULE · ORAL
Active ingredientsEMTRICITABINE (200 mg/1)
Marketing started20200831
Package count2

External sources

Source: openFDA. Public-domain (CC0).