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Guaifenesin 600 mg

NDC 25000-042 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerMARKSANS PHARMA LIMITED
Marketing categoryAbbreviated NDA (generic) · App ANDA217780
Dosage form / routeTABLET · ORAL
Active ingredientsGUAIFENESIN (600 mg/1)
Marketing started20230823
Package count4

External sources

Source: openFDA. Public-domain (CC0).