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GUAIFENESIN

NDC 79903-124 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Generic nameGuaifenesin
Labeler / ManufacturerWalmart Stores, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209254
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsGUAIFENESIN (600 mg/1)
Marketing started20220428
Package count1

External sources

Source: openFDA. Public-domain (CC0).