NDC 65162-065

Sodium Oxybate 500 mg per 1 mL solution

On the label: Amneal Pharmaceuticals.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Amneal Pharmaceuticals LLCBranchburg, NJ, United StatesMakes it, tests it, packages it and labels it No problems foundAug 28, 2026 · 9 inspections

Product details

Generic drug
4-Hydroxybutanoic Acid: every company that makes it
Form
solution, oral
Strength
500 mg per 1 mL
Approval
ANDA ANDA203631
On the market since
Sep 12, 2025
Package NDCs
65162-065-87
Official label
DailyMed (National Library of Medicine), updated May 19, 2025

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