Pregabalin
- Product NDC
- 70518-2571
- 11-digit product format
- 705182571
- Labeler code
- 70518
- Product ID
- 70518-2571_f0826469-8b81-7a27-e053-2995a90a8378
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pregabalin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA209743
- Marketing category
- ANDA
- Marketing start
- 2020-02-07
- Marketing end
- 0000-00-00
- Substance
- PREGABALIN
- Active strength
- 50 mg/1
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2571 | PREGABALIN CAPSULE [REMEDYREPACK INC.] | 11 | Legacy NDC | 20250321_814a5454-311d-47e9-9e69-d7eb3db65bc6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2571-0 | 70518257100 | 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2571-0) | 90 capsule | 2020-02-07 | 0000-00-00 | No | No | Current |
| 70518-2571-1 | 70518257101 | 60 CAPSULE in 1 BOTTLE, PLASTIC (70518-2571-1) | 60 capsule | 2021-12-09 | 0000-00-00 | No | No | Current |