NDC 68071-3798
Acetaminophen and Codeine Phosphate 30 mg / 300 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Elite Laboratories, Inc.'s NDC 64850-642.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Elite Laboratories, Inc. | Northvale, NJ, United States | Makes it and labels it | Problems found, fixed voluntarilyAug 1, 2025 · 12 inspections, 1 with FDA action |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Acetaminophen and Codeine: every company that makes it
- Form
- tablet, oral
- Strength
- 30 mg / 300 mg
- Approval
- ANDA ANDA212418
- On the market since
- Sep 10, 2019
- Package NDCs
68071-3798-6- Official label
- DailyMed (National Library of Medicine), updated Feb 19, 2025
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