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Guaifenesin

NDC 68196-405 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerSAM'S WEST INC
Marketing categoryAbbreviated NDA (generic) · App ANDA213420
Dosage form / routeTABLET · ORAL
Active ingredientsGUAIFENESIN (1200 mg/1)
Marketing started20231006
Package count1

External sources

Source: openFDA. Public-domain (CC0).