PREGABALIN
- Product NDC
- 55700-956
- 11-digit product format
- 557000956
- Labeler code
- 55700
- Product ID
- 55700-956_799897af-12c1-42de-a3aa-bea785a95262
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREGABALIN
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA213226
- Marketing category
- ANDA
- Marketing start
- 2021-12-21
- Marketing end
- 0000-00-00
- Substance
- PREGABALIN
- Active strength
- 165 mg/1
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-956-30 | 55700095630 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55700-956-30) | 2021-12-21 | 0000-00-00 | No | No | Current |