NDC 68071-3447

Hydrocodone Bitartrate and Acetaminophen 5 mg / 325 mg tablet

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.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
68071-3447-3
Official label
DailyMed (National Library of Medicine), updated Feb 5, 2025

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