NDC 70934-555

Hydrocodone Bitartrate and Acetaminophen 5 mg / 325 mg tablet

On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Aurolife Pharma LLC's NDC 13107-019.

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
Strength
5 mg / 325 mg
Approval
ANDA ANDA201013
On the market since
Feb 17, 2020
Package NDCs
70934-555-15 70934-555-30
Official label
DailyMed (National Library of Medicine), updated Aug 25, 2020

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