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Guaifenesin

NDC 46122-750 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerAMERISOURCE BERGEN
Marketing categoryAbbreviated NDA (generic) · App ANDA209254
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsGUAIFENESIN (600 mg/1)
Marketing started20230811
Package count1

External sources

Source: openFDA. Public-domain (CC0).