FDA NDC Directory · JSON-LD · Markdown

GUAIFENESIN

NDC 51316-071 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Generic nameguaifenesin
Labeler / ManufacturerCVS
Marketing categoryAbbreviated NDA (generic) · App ANDA209254
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsGUAIFENESIN (600 mg/1)
Marketing started20221007
Package count1

External sources

Source: openFDA. Public-domain (CC0).