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Guaifenesin and Pseudoephedrine Hydrochloride

NDC 41415-994 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerPUBLIX SUPER MARKETS, INC
Marketing categoryAbbreviated NDA (generic) · App ANDA212542
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsGUAIFENESIN (600 mg/1)
PSEUDOEPHEDRINE HYDROCHLORIDE (60 mg/1)
Marketing started20220407
Package count2

External sources

Source: openFDA. Public-domain (CC0).