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GUAIFENESIN

NDC 68196-960 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerSam's West Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA210453
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsGUAIFENESIN (1200 mg/1)
Marketing started20250731
Package count1

External sources

Source: openFDA. Public-domain (CC0).