Pregabalin
- Product NDC
- 47335-689
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pregabalin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- ANDA091157
- Marketing category
- ANDA
- Substance
- PREGABALIN
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 47335-689-08 | 100 CAPSULE in 1 BOTTLE (47335-689-08) | 2019-12-04 | | No | Historical |
| 47335-689-18 | 1000 CAPSULE in 1 BOTTLE (47335-689-18) | 2019-12-04 | | No | Historical |
| 47335-689-83 | 30 CAPSULE in 1 BOTTLE (47335-689-83) | 2019-12-04 | | No | Historical |
| 47335-689-88 | 100 CAPSULE in 1 BOTTLE (47335-689-88) | 2019-12-04 | | No | Historical |