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Ibuprofen

NDC 37835-581 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerBi-Mart
Marketing categoryAbbreviated NDA (generic) · App ANDA079174
Dosage form / routeTABLET · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20110101
Package count4

External sources

Source: openFDA. Public-domain (CC0).