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IBUPROFEN Infants

NDC 51672-2146 · HUMAN OTC DRUG · SUSPENSION/ DROPS

Generic nameIBUPROFEN
Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217261
Dosage form / routeSUSPENSION/ DROPS · ORAL
Active ingredientsIBUPROFEN (50 mg/1.25mL)
Marketing started20230808
Package count2

External sources

Source: openFDA. Public-domain (CC0).