Pregabalin 69367-0430
Product NDC
69367-0430- Manufacturer
- Westminster Pharmaceuticals, Llc
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CV
- Marketing Start
- November 17, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA212988
Active Ingredients
| Ingredient | Strength |
|---|---|
| Pregabalin | 225 mg/1 |
Packaging Options(2)
500 CAPSULE in 1 BOTTLE (69367-430-05)
90 CAPSULE in 1 BOTTLE (69367-430-09)