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Guaifenesin

NDC 69848-017 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerGRANULES USA, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA213420
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsGUAIFENESIN (600 mg/1)
Marketing started20211231
Package count1

External sources

Source: openFDA. Public-domain (CC0).