FDA NDC Directory · JSON-LD · Markdown

Guaifenesin

NDC 73581-400 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerYYBA CORP
Marketing categoryAbbreviated NDA (generic) · App ANDA209215
Dosage form / routeTABLET · ORAL
Active ingredientsGUAIFENESIN (600 mg/1)
Marketing started20260310
Package count1

External sources

Source: openFDA. Public-domain (CC0).