NDC 0245-0411
Hydrocodone Bitartrate and Acetaminophen 325 mg / 7.5 mg tablet
On the label: Upsher-Smith Laboratories, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bora Pharmaceuticals Inc. | Maple Grove, MN, United States | Makes it and packages it | Problems found, fixed voluntarilyAug 30, 2022 · 16 inspections |
Product details
- Generic drug
- Acetaminophen and Hydrocodone: every company that makes it
- Form
- tablet, oral
- Strength
- 325 mg / 7.5 mg
- Approval
- ANDA ANDA206484
- On the market since
- Mar 27, 2017
- Package NDCs
0245-0411-010245-0411-110245-0411-500245-0411-89- Official label
- DailyMed (National Library of Medicine), updated Jul 14, 2025
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