United States · FDA National Drug Code directory
Sodium Oxybate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 65162-065_fb0e7d54-bf58-46d7-8561-9a270771f0d2
- Product NDC
- 65162-065
- Form
- SOLUTION
- Composition / generic term
- Sodium Oxybate
- Labeler
- Amneal Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250912
- Source listing expiry
- 20271231
Source-listed ingredients
- SODIUM OXYBATE — 500 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (65162-065-87) / 180 mL in 1 BOTTLE · 65162-065-87
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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