Pregabalin
- Product NDC
- 70518-2980
- 11-digit product format
- 705182980
- Labeler code
- 70518
- Product ID
- 70518-2980_e5fc24c8-8974-89df-e053-2a95a90a5669
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pregabalin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA209743
- Marketing category
- ANDA
- Marketing start
- 2021-01-06
- Marketing end
- 0000-00-00
- Substance
- PREGABALIN
- Active strength
- 225 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 |
|---|
| 70518-2980 | PREGABALIN CAPSULE [REMEDYREPACK INC.] | 9 | Legacy NDC | 20250409_9111d695-9f3a-4b07-9daa-c1339b16acb3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2980-0 | 70518298000 | 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2980-0) | 90 capsule | 2021-01-06 | 0000-00-00 | No | No | Current |