Pregabalin
- Product NDC
- 63304-049
- 11-digit product format
- 633040049
- Labeler code
- 63304
- Product ID
- 63304-049_50c7518b-349e-4284-ac0c-1ac2c332c3e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pregabalin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- ANDA211889
- 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
- 2023-12-31
- 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 |
|---|
| 63304-049-30 | 63304004930 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-049-30) | 2021-04-13 | 0000-00-00 | No | No | Current |