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Pseudoephedrine hydrochloride

NDC 51660-204 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerOhm Laboratories Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077442
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPSEUDOEPHEDRINE HYDROCHLORIDE (120 mg/1)
Marketing started20060428
Package count2

External sources

Source: openFDA. Public-domain (CC0).