PREGABALIN
- Product NDC
- 72189-115
- 11-digit product format
- 721890115
- Labeler code
- 72189
- Product ID
- 72189-115_2be8eb66-533f-0815-e063-6294a90a115d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREGABALIN
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA209743
- Marketing category
- ANDA
- Marketing start
- 2020-07-22
- Substance
- PREGABALIN
- Active strength
- 25 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 |
|---|
| 72189-115-90 | 72189011590 | 90 CAPSULE in 1 BOTTLE (72189-115-90) | 90 capsule | 2020-07-23 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| PREGABALIN | Direct_Rx | 2025-01-17 | HUMAN PRESCRIPTION DRUG LABEL | 13 |