FDA NDC Directory · JSON-LD · Markdown

BACLOFEN

NDC 68788-8737 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214374
Dosage form / routeTABLET · ORAL
Active ingredientsBACLOFEN (20 mg/1)
Marketing started20240916
Package count5

External sources

Source: openFDA. Public-domain (CC0).