FDA NDC Directory · JSON-LD · Markdown

Ibuprofen

NDC 75907-428 · HUMAN OTC DRUG · TABLET, COATED

Labeler / ManufacturerDr. Reddy's Laboratories Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA079174
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20260701
Package count1

External sources

Source: openFDA. Public-domain (CC0).