NDC 43386-352
Hydrocodone Bitartrate and Acetaminophen 300 mg / 7.5 mg tablet
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Novel Laboratories, Inc. | Somerset, NJ, United States | Makes it and tests it | Problems found, fixed voluntarilyApr 17, 2026 · 15 inspections, 1 with FDA action |
Product details
- Generic drug
- Acetaminophen and Hydrocodone: every company that makes it
- Form
- tablet, oral
- Strength
- 300 mg / 7.5 mg
- Approval
- ANDA ANDA206142
- On the market since
- Nov 14, 2016
- Package NDCs
43386-352-0143386-352-0343386-352-05- Official label
- DailyMed (National Library of Medicine), updated Feb 15, 2024
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