NDC 68788-8882

Acetaminophen And Codeine Phosphate 60 mg / 300 mg tablet

On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Eywa Pharma Inc's NDC 71930-056.

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
60 mg / 300 mg
Approval
ANDA ANDA211610
On the market since
Jun 2, 2025
Package NDCs
68788-8882-1 68788-8882-3 68788-8882-6
Official label
DailyMed (National Library of Medicine), updated Jun 2, 2025

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