Pregabalin
- Product NDC
- 59762-1351
- 11-digit product format
- 597621351
- Labeler code
- 59762
- Product ID
- 59762-1351_29b32120-149b-4620-9932-28e1f919627a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pregabalin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Greenstone LLC
- Application
- NDA021446
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-07-19
- Marketing end
- 0000-00-00
- Substance
- PREGABALIN
- Active strength
- 150 mg/1
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59762-1351 | PREGABALIN CAPSULE PREGABALIN SOLUTION [MYLAN PHARMACEUTICALS INC.] | 12 | Legacy NDC | 20250503_ebe34db4-816d-4f0a-adbb-826693662754.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59762-1351-1 | 59762135101 | 90 CAPSULE in 1 BOTTLE (59762-1351-1) | 90 capsule | 2019-07-19 | 0000-00-00 | No | No | Current |