NDC 68071-3651

Acetaminophen And Codeine Phosphate 30 mg / 300 mg tablet

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Eywa Pharma Inc's NDC 71930-055.

United States: 1

Where the pills inside were made

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

Repackaging site

Product details

Generic drug
Acetaminophen and Codeine: every company that makes it
Form
tablet, oral
Strength
30 mg / 300 mg
Approval
ANDA ANDA211610
On the market since
Aug 2, 2019
Package NDCs
68071-3651-6
Official label
DailyMed (National Library of Medicine), updated Jul 24, 2024

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