Pregabalin
- Product NDC
- 71335-2030
- 11-digit product format
- 713352030
- Labeler code
- 71335
- Product ID
- 71335-2030_93aa6727-1c18-4876-9a58-aff93193e577
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- pregabalin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212865
- Marketing category
- ANDA
- Marketing start
- 2020-03-31
- Marketing end
- 0000-00-00
- Substance
- PREGABALIN
- Active strength
- 150 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-2030-1 | 71335203001 | 30 CAPSULE in 1 BOTTLE (71335-2030-1) | 30 capsule | 2022-02-10 | 0000-00-00 | No | No | Current |
| 71335-2030-2 | 71335203002 | 60 CAPSULE in 1 BOTTLE (71335-2030-2) | 60 capsule | 2022-02-10 | 0000-00-00 | No | No | Current |
| 71335-2030-3 | 71335203003 | 90 CAPSULE in 1 BOTTLE (71335-2030-3) | 90 capsule | 2022-02-10 | 0000-00-00 | No | No | Current |
| 71335-2030-4 | 71335203004 | 180 CAPSULE in 1 BOTTLE (71335-2030-4) | 180 capsule | 2022-02-10 | 0000-00-00 | No | No | Current |