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Guaifenesin and Dextromethorphan HBr

NDC 51660-301 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerOHM LABORATORIES INC
Marketing categoryAbbreviated NDA (generic) · App ANDA214781
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsDEXTROMETHORPHAN HYDROBROMIDE (30 mg/1)
GUAIFENESIN (600 mg/1)
Marketing started20210701
Package count2

External sources

Source: openFDA. Public-domain (CC0).