NDC 61919-556

Pentazocine Hydrochloride And Naloxone Hydrochloride 50 mg / 0.5 mg tablet

On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 43386-680.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Novel Laboratories, Inc.Somerset, NJ, United StatesMakes it and tests it Problems found, fixed voluntarilyApr 17, 2026 · 15 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Naloxone and Pentazocine: every company that makes it
Form
tablet
Strength
50 mg / 0.5 mg
Approval
ANDA ANDA075735
On the market since
Jan 1, 2014
Package NDCs
61919-556-30
Official label
DailyMed (National Library of Medicine), updated Nov 10, 2016

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