NDC 68071-2664
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.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Wes Pharma Inc | Westminster, MD, United States | Makes it, packages it and labels it | Problems found, fixed voluntarilyNov 20, 2025 · 7 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Acetaminophen and Hydrocodone: every company that makes it
- Form
- tablet
- Strength
- 5 mg / 325 mg
- Approval
- ANDA ANDA210211
- On the market since
- Jul 13, 2018
- Package NDCs
68071-2664-268071-2664-6- Official label
- DailyMed (National Library of Medicine), updated May 27, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?