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Guaifenesin and Dextromethorphan HBr

NDC 63304-110 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerSUN PHARMACEUTICAL INDUSTRIES, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA214781
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsDEXTROMETHORPHAN HYDROBROMIDE (60 mg/1)
GUAIFENESIN (1200 mg/1)
Marketing started20210701
Package count1

External sources

Source: openFDA. Public-domain (CC0).