NDC 69986-015
Pregabalin 330 mg tablet, film coated, extended release
On the label: Sinotherapeutics Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Haimen Pharma Inc. | Nantong, China | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyAug 25, 2023 · 2 inspections |
Product details
- Generic drug
- Pregabalin: every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 330 mg
- Approval
- ANDA ANDA214496
- On the market since
- Nov 30, 2023
- Package NDCs
69986-015-01- Official label
- DailyMed (National Library of Medicine), updated Jun 6, 2023
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