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Ibuprofen and Pseudoephedrine Hydrochloride

NDC 58602-839 · HUMAN OTC DRUG · TABLET, COATED

Labeler / ManufacturerAurohealth LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA213565
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
PSEUDOEPHEDRINE HYDROCHLORIDE (30 mg/1)
Marketing started20230310
Package count1

External sources

Source: openFDA. Public-domain (CC0).