# Sodium Oxybate

NDC: 65162-065
Generic name: Sodium Oxybate
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20250912

FDA application: ANDA203631

## Active ingredients

- SODIUM OXYBATE: 500 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65162-065"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65162-065
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5a9e9045-f04d-46eb-8396-2495c6090a31