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Guaifenesin Extended-Release 600 mg

NDC 53041-233 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Generic nameGuaifenesin
Labeler / ManufacturerGuardian Drug Company
Marketing categoryAbbreviated NDA (generic) · App ANDA209215
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsGUAIFENESIN (600 mg/1)
Marketing started20180301
Package count3

External sources

Source: openFDA. Public-domain (CC0).