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GUAIFENESIN

NDC 82804-265 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA213420
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsGUAIFENESIN (600 mg/1)
Marketing started20220819
Package count1

External sources

Source: openFDA. Public-domain (CC0).