FDA NDC Directory · JSON-LD · Markdown

Guaifenesin

NDC 21130-554 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerSafeway, Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA213420
Dosage form / routeTABLET · ORAL
Active ingredientsGUAIFENESIN (1200 mg/1)
Marketing started20230630
Package count1

External sources

Source: openFDA. Public-domain (CC0).