NDC 53217-266

Hydrocodone Bitartrate and Acetaminophen 325 mg / 7.5 mg tablet

On the label: Aidarex Pharmaceuticals LLC. It's repackaged: Aidarex Pharmaceuticals LLC 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

Product details

Generic drug
Acetaminophen and Hydrocodone: every company that makes it
Form
tablet
Strength
325 mg / 7.5 mg
Approval
ANDA ANDA201013
On the market since
Nov 30, 2016
Package NDCs
53217-266-12 53217-266-15 53217-266-20 53217-266-24 53217-266-30 53217-266-60 53217-266-90
Official label
DailyMed (National Library of Medicine), updated Apr 7, 2017

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