Pregabalin
- Product NDC
- 82804-170
- 11-digit product format
- 828040170
- Labeler code
- 82804
- Product ID
- 82804-170_e80b626b-701e-4b20-a6b3-77b064c8d495
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pregabalin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA206912
- Marketing category
- ANDA
- Marketing start
- 2019-10-08
- Substance
- PREGABALIN
- Active strength
- 75 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 |
|---|
| 82804-170-60 | 82804017060 | 60 CAPSULE in 1 BOTTLE (82804-170-60) | 60 capsule | 2024-12-03 | No | No | Historical |
| 82804-170-90 | 82804017090 | 90 CAPSULE in 1 BOTTLE (82804-170-90) | 90 capsule | 2025-03-26 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pregabalin | Proficient Rx LP | 2025-03-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |