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Ibuprofen

NDC 70518-4786 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA202413
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (400 mg/1)
Marketing started20261028
Package count1

External sources

Source: openFDA. Public-domain (CC0).