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Guaifenesin

NDC 69842-335 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerCVS PHARMACY, INC
Marketing categoryAbbreviated NDA (generic) · App ANDA213420
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsGUAIFENESIN (1200 mg/1)
Marketing started20210301
Package count3

External sources

Source: openFDA. Public-domain (CC0).