NDC 71335-2118

Hydrocodone Bitartrate and Acetaminophen 10 mg / 325 mg tablet

On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-997.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Ascent Pharmaceuticals IncCentral Islip, NY, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyAug 9, 2024 · 9 inspections

Repackaging site

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Acetaminophen and Hydrocodone: every company that makes it
Form
tablet, oral
Strength
10 mg / 325 mg
Approval
ANDA ANDA211487
On the market since
Nov 8, 2018
Package NDCs
71335-2118-0 71335-2118-1 71335-2118-2 71335-2118-3 71335-2118-4 71335-2118-5 71335-2118-6 71335-2118-7 71335-2118-8 71335-2118-9
Official label
DailyMed (National Library of Medicine), updated Oct 21, 2025

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