NDC 76420-821
Acetaminophen And Codeine Phosphate 30 mg / 300 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Eywa Pharma Inc's NDC 71930-055.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Wes Pharma Inc | Westminster, MD, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyNov 20, 2025 · 7 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
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
76420-821-0076420-821-0176420-821-0376420-821-0576420-821-1076420-821-1276420-821-1576420-821-2076420-821-2476420-821-3076420-821-5076420-821-60- Official label
- DailyMed (National Library of Medicine), updated Aug 17, 2025
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