FDA NDC Directory · JSON-LD · Markdown

IBUPROFEN 200 MG

NDC 0761-0908 · HUMAN OTC DRUG · TABLET

Generic nameIBUPROFEN
Labeler / ManufacturerBasic Drugs, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA079174
Dosage form / routeTABLET · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20211214
Package count1

External sources

Source: openFDA. Public-domain (CC0).