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Pseudoephedrine Hydrochloride

NDC 68016-204 · HUMAN OTC DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerChain Drug Consortium, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077442
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsPSEUDOEPHEDRINE HYDROCHLORIDE (120 mg/1)
Marketing started20060428
Package count1

External sources

Source: openFDA. Public-domain (CC0).