FDA NDC Directory · JSON-LD · Markdown

Sodium phenylbutyrate

NDC 70710-2180 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA220418
Dosage form / routeTABLET · ORAL
Active ingredientsSODIUM PHENYLBUTYRATE (500 mg/1)
Marketing started20260323
Package count1

External sources

Source: openFDA. Public-domain (CC0).