Pregabalin
- Product NDC
- 71335-2012
- 11-digit product format
- 713352012
- Labeler code
- 71335
- Product ID
- 71335-2012_21eee03b-b9aa-4564-955f-b31c584adb15
- 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
- 100 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 |
|---|
| 71335-2012-1 | 71335201201 | 30 CAPSULE in 1 BOTTLE (71335-2012-1) | 30 capsule | 2022-02-10 | 0000-00-00 | No | No | Current |
| 71335-2012-2 | 71335201202 | 90 CAPSULE in 1 BOTTLE (71335-2012-2) | 90 capsule | 2022-02-10 | 0000-00-00 | No | No | Current |
| 71335-2012-3 | 71335201203 | 60 CAPSULE in 1 BOTTLE (71335-2012-3) | 60 capsule | 2022-02-10 | 0000-00-00 | No | No | Current |