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Ibuprofen

NDC 68210-4192 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerSpirit Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA079174
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20211208
Package count1

External sources

Source: openFDA. Public-domain (CC0).