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IBUPROFEN

NDC 29485-9291 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameIBUPROFEN 200MG
Labeler / ManufacturerLil' Drug Store Products, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075010
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20170502
Marketing ended20270618
Package count2

External sources

Source: openFDA. Public-domain (CC0).