NDC 31722-997
Hydrocodone Bitartrate and Acetaminophen 10 mg / 325 mg tablet
On the label: Camber Pharmaceuticals Inc..
Where it's 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 |
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, oral
- Strength
- 10 mg / 325 mg
- Approval
- ANDA ANDA211487
- On the market since
- Nov 8, 2018
- Package NDCs
31722-997-0131722-997-05- Official label
- DailyMed (National Library of Medicine), updated Aug 21, 2025
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