PREGABALIN
- Product NDC
- 69539-129
- 11-digit product format
- 695390129
- Labeler code
- 69539
- Product ID
- 69539-129_912e357e-eaaf-403c-b5a8-3b5b65f0656d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREGABALIN
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- MSN LABORATORIES PRIVATE LIMITED
- Application
- ANDA213226
- Marketing category
- ANDA
- Marketing start
- 2021-04-13
- Marketing end
- 0000-00-00
- Substance
- PREGABALIN
- Active strength
- 330 mg/1
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 69539-129 | PREGABALIN TABLET, FILM COATED, EXTENDED RELEASE [MSN LABORATORIES PRIVATE LIMITED] | 4 | Legacy NDC | 20210526_b62cadf7-3c0c-4239-9e9a-c0f6921047b1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69539-129-30 | 69539012930 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69539-129-30) | 2021-04-13 | 0000-00-00 | No | No | Current |