NDC 71335-0108

Hydrocodone Bitartrate and Acetaminophen 325 mg / 7.5 mg tablet

On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Aurolife Pharma LLC's NDC 13107-020.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Aurolife Pharma LLCDayton, NJ, United StatesMakes it, tests it, packages it and labels it Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Acetaminophen and Hydrocodone: every company that makes it
Form
tablet, oral
Strength
325 mg / 7.5 mg
Approval
ANDA ANDA201013
On the market since
Apr 11, 2012
Package NDCs
71335-0108-0 71335-0108-1 71335-0108-2 71335-0108-3 71335-0108-4 71335-0108-5 71335-0108-6 71335-0108-7 71335-0108-8 71335-0108-9
Official label
DailyMed (National Library of Medicine), updated Oct 8, 2024

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