Lyrica CR
- Product NDC
- 63539-024
- 11-digit product format
- 635390024
- Labeler code
- 63539
- Product ID
- 63539-024_ee853b26-626b-459d-b6ef-ef62fa123828
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREGABALIN
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- U.S. Pharmaceuticals
- Application
- NDA209501
- Marketing category
- NDA
- Marketing start
- 2016-01-01
- Marketing end
- 0000-00-00
- Substance
- PREGABALIN
- Active strength
- 165 mg/1
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63539-024-02 | 63539002402 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63539-024-02) | 2016-01-01 | 0000-00-00 | No | No | Current |