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ibuprofen

NDC 45802-897 · HUMAN OTC DRUG · SUSPENSION

Generic nameIbuprofen
Labeler / ManufacturerPadagis Israel Pharmaceuticals Ltd
Marketing categoryAbbreviated NDA (generic) · App ANDA074937
Dosage form / routeSUSPENSION · ORAL
Active ingredientsIBUPROFEN (100 mg/5mL)
Marketing started20111117
Package count2

External sources

Source: openFDA. Public-domain (CC0).