FDA NDC Directory · JSON-LD · Markdown

Guaifenesin and Dextromethorphan HBr

NDC 57483-114 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerINNOVUS PHARMACEUTICALS, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA206941
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsGUAIFENESIN (1200 mg/1)
DEXTROMETHORPHAN HYDROBROMIDE (60 mg/1)
Marketing started20261027
Package count1

External sources

Source: openFDA. Public-domain (CC0).