NDC 0406-0124
Hydrocodone Bitartrate And Acetaminophen 325 mg / 7.5 mg tablet
On the label: SpecGx LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| SpecGx LLC | Hobart, NY, United States | Makes it and tests it | No problems foundMar 13, 2020 · 6 inspections |
| SpecGx LLC | St. Louis, MO, United States | Makes the active ingredient | Problems found, fixed voluntarilyOct 22, 2025 · 8 inspections |
| SpecGx LLC | Greenville, IL, United States | Makes the active ingredient | Problems found, fixed voluntarilyFeb 27, 2026 · 5 inspections |
Product details
- Generic drug
- Acetaminophen and Hydrocodone: every company that makes it
- Form
- tablet, oral
- Strength
- 325 mg / 7.5 mg
- Approval
- ANDA ANDA040405
- On the market since
- Sep 8, 2000
- Package NDCs
0406-0124-010406-0124-050406-0124-100406-0124-120406-0124-200406-0124-230406-0124-300406-0124-600406-0124-620406-0124-90- Official label
- DailyMed (National Library of Medicine), updated Apr 20, 2026
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