NDC 67296-2201

Hydrocodone Bitartrate and Acetaminophen 5 mg / 325 mg tablet

On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Eywa Pharma Inc's NDC 71930-019.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Wes Pharma IncWestminster, MD, United StatesMakes it, packages it and labels it Problems found, fixed voluntarilyNov 20, 2025 · 7 inspections

Repackaging site

Product details

Generic drug
Acetaminophen and Hydrocodone: every company that makes it
Form
tablet, oral
Strength
5 mg / 325 mg
Approval
ANDA ANDA210211
On the market since
Jul 13, 2018
Package NDCs
67296-2201-1 67296-2201-2 67296-2201-3 67296-2201-4 67296-2201-5 67296-2201-6 67296-2201-7 67296-2201-8
Official label
DailyMed (National Library of Medicine), updated Mar 3, 2026

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