Pregabalin
- Product NDC
- 82804-188
- 11-digit product format
- 828040188
- Labeler code
- 82804
- Product ID
- 82804-188_efc36145-fffd-44de-9a42-f277d0ff39c9
- 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
- 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 |
|---|
| 82804-188-60 | 82804018860 | 60 CAPSULE in 1 BOTTLE (82804-188-60) | 60 capsule | 2025-01-17 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pregabalin | Proficient Rx LP | 2025-01-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |