FDA NDC Directory · JSON-LD · Markdown

Ibuprofen

NDC 76420-577 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAsclemed USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213794
Dosage form / routeTABLET · ORAL
Active ingredientsIBUPROFEN (800 mg/1)
Marketing started20200508
Package count4

External sources

Source: openFDA. Public-domain (CC0).