NDC 68071-2721

Naltrexone Hydrochloride 50 mg tablet, film coated

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Accord Healthcare Inc.'s NDC 16729-081.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Intas Pharmaceuticals LimitedAhmedabad, IndiaMakes it and tests it No problems foundJul 12, 2024 · 10 inspections

Repackaging site

Product details

Generic drug
Naltrexone: every company that makes it
Form
tablet, film coated
Strength
50 mg
Approval
ANDA ANDA091205
On the market since
Jan 18, 2012
Package NDCs
68071-2721-3
Official label
DailyMed (National Library of Medicine), updated May 20, 2022

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