Pregabalin 76420-0122
Product NDC
76420-0122- Manufacturer
- Asclemed Usa, Inc.
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CV
- Marketing Start
- July 19, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA210432
Active Ingredients
| Ingredient | Strength |
|---|---|
| Pregabalin | 200 mg/1 |
Packaging Options(3)
30 CAPSULE in 1 BOTTLE (76420-122-30)
60 CAPSULE in 1 BOTTLE (76420-122-60)
90 CAPSULE in 1 BOTTLE (76420-122-90)