Pregabalin
- Product NDC
- 82804-247
- 11-digit product format
- 828040247
- Labeler code
- 82804
- Product ID
- 82804-247_7d25bec8-b503-4f63-8995-372a6df58c72
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pregabalin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA209357
- Marketing category
- ANDA
- Marketing start
- 2019-07-19
- Substance
- PREGABALIN
- Active strength
- 100 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 |
|---|
| 82804-247-90 | 82804024790 | 90 CAPSULE in 1 BOTTLE (82804-247-90) | 90 capsule | 2025-10-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pregabalin | Proficient Rx LP | 2025-10-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |