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Ibuprofen

NDC 55910-768 · HUMAN OTC DRUG · TABLET, COATED

Labeler / ManufacturerDolgencorp, Inc. (DOLLAR GENERAL & REXALL)
Marketing categoryAbbreviated NDA (generic) · App ANDA079174
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20170430
Marketing ended20261230
Package count1

External sources

Source: openFDA. Public-domain (CC0).