FDA NDC Directory · JSON-LD · Markdown

Sodium Oxybate

NDC 65162-065 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA203631
Dosage form / routeSOLUTION · ORAL
Active ingredientsSODIUM OXYBATE (500 mg/mL)
Marketing started20250912
Package count1

External sources

Source: openFDA. Public-domain (CC0).