NDC 68071-2668
Hydrocodone Bitartrate and Acetaminophen 5 mg / 325 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-996.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ascent Pharmaceuticals Inc | Central Islip, NY, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyAug 9, 2024 · 9 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Recalls
- Nov 19, 2021 · Class II · Ascent Pharmaceuticals, Inc.
Product Mix-up
Lots: Lot #: 21070817, Exp 6/2023
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Acetaminophen and Hydrocodone: every company that makes it
- Form
- tablet
- Strength
- 5 mg / 325 mg
- Approval
- ANDA ANDA211487
- On the market since
- Nov 8, 2018
- Package NDCs
68071-2668-268071-2668-468071-2668-6- Official label
- DailyMed (National Library of Medicine), updated Mar 31, 2022
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