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Guaifenesin Extended-Release

NDC 68094-048 · HUMAN OTC DRUG · TABLET, MULTILAYER, EXTENDED RELEASE

Generic nameGuaifenesin
Labeler / ManufacturerPrecision Dose Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078912
Dosage form / routeTABLET, MULTILAYER, EXTENDED RELEASE · ORAL
Active ingredientsGUAIFENESIN (600 mg/1)
Marketing started20230322
Package count1

External sources

Source: openFDA. Public-domain (CC0).