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Guaifenesin and Pseudoephedrine Hydrochloride

NDC 62011-0475 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerSTRATEGIC SOURCING SERVICES LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212542
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsGUAIFENESIN (600 mg/1)
PSEUDOEPHEDRINE HYDROCHLORIDE (60 mg/1)
Marketing started20171115
Package count1

External sources

Source: openFDA. Public-domain (CC0).