Pregabalin
- Product NDC
- 71205-696
- 11-digit product format
- 712050696
- Labeler code
- 71205
- Product ID
- 71205-696_137ffe30-ff8b-409d-a719-6be19d4d9522
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pregabalin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA208677
- Marketing category
- ANDA
- Marketing start
- 2021-08-24
- Substance
- PREGABALIN
- Active strength
- 50 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 |
|---|
| 71205-696-30 | 71205069630 | 30 CAPSULE in 1 BOTTLE (71205-696-30) | 30 capsule | 2023-10-30 | No | No | Historical |
| 71205-696-60 | 71205069660 | 60 CAPSULE in 1 BOTTLE (71205-696-60) | 60 capsule | 2023-10-30 | No | No | Historical |
| 71205-696-90 | 71205069690 | 90 CAPSULE in 1 BOTTLE (71205-696-90) | 90 capsule | 2023-10-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pregabalin | Proficient Rx LP | 2023-10-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |