PREGABALIN
- Product NDC
- 72162-2304
- 11-digit product format
- 721622304
- Labeler code
- 72162
- Product ID
- 72162-2304_250c155b-3d38-41f9-945b-e983a206e583
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREGABALIN
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210432
- Marketing category
- ANDA
- Marketing start
- 2019-07-19
- Substance
- PREGABALIN
- Active strength
- 150 mg/1
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 55JG375S6M | PREGABALIN | 148553-50-8 | PREGABALIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2304-0 | 72162230400 | 1000 CAPSULE in 1 BOTTLE (72162-2304-0) | 1000 capsule | 2024-04-30 | No | No | Historical |
| 72162-2304-9 | 72162230409 | 90 CAPSULE in 1 BOTTLE (72162-2304-9) | 90 capsule | 2024-04-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| PREGABALIN | Bryant Ranch Prepack | 2025-11-06 | HUMAN PRESCRIPTION DRUG LABEL | 101 |
| PREGABALIN | Bryant Ranch Prepack | 2024-04-30 | HUMAN PRESCRIPTION DRUG LABEL | 100 |