FDA NDC Directory · JSON-LD · Markdown

ibuprofen

NDC 55910-901 · HUMAN OTC DRUG · TABLET, COATED

Labeler / ManufacturerDOLGENCORP INC
Marketing categoryAbbreviated NDA (generic) · App ANDA091239
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20191209
Package count1

External sources

Source: openFDA. Public-domain (CC0).