NDC 65162-065 – Sodium Oxybate

Sodium Oxybate 500 mg/mL · Solution · Oral

Human Prescription Drug DEA schedule CIII

Product NDC65162-065

Product details

Brand name
Sodium Oxybate
Generic name
Sodium Oxybate
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA203631
Marketed since
September 12, 2025
Listing expires
December 31, 2027
Pharmacologic class
Central Nervous System Depressant

Active ingredients

Uses, dosage, side effects and warnings for sodium oxybate →

Package NDC codes (1)

Package NDCDescriptionSince
65162-065-871 BOTTLE in 1 CARTON (65162-065-87) / 180 mL in 1 BOTTLESep 12, 2025

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