FDA NDC Directory · JSON-LD · Markdown

MUCUS RELIEF

NDC 73581-403 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Generic nameGUAIFENESIN
Labeler / ManufacturerYYBA Corp
Marketing categoryAbbreviated NDA (generic) · App ANDA209215
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsGUAIFENESIN (1200 mg/1)
Marketing started20260701
Package count2

External sources

Source: openFDA. Public-domain (CC0).