Pregabalin 47335-0691
Product NDC
47335-0691- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CV
- Marketing Start
- December 4, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA091157
Active Ingredients
| Ingredient | Strength |
|---|---|
| Pregabalin | 200 mg/1 |
Packaging Options(4)
100 CAPSULE in 1 BOTTLE (47335-691-08)
1000 CAPSULE in 1 BOTTLE (47335-691-18)
30 CAPSULE in 1 BOTTLE (47335-691-83)
100 CAPSULE in 1 BOTTLE (47335-691-88)