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Baclofen

NDC 70710-1666 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Pharmaceuticals (USA) Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211659
Dosage form / routeTABLET · ORAL
Active ingredientsBACLOFEN (15 mg/1)
Marketing started20240620
Package count1

External sources

Source: openFDA. Public-domain (CC0).