Pregabalin 72205-0079
Product NDC
72205-0079- Manufacturer
- Novadoz Pharmaceuticals Llc
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CV
- Marketing Start
- April 13, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA213226
Active Ingredients
| Ingredient | Strength |
|---|---|
| Pregabalin | 330 mg/1 |
Packaging Options(1)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72205-079-30)