Pregabalin
- Product NDC
- 70518-2364
- 11-digit product format
- 705182364
- Labeler code
- 70518
- Product ID
- 70518-2364_ea3aafc5-7ea3-5ee3-e053-2a95a90a929d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pregabalin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA209743
- Marketing category
- ANDA
- Marketing start
- 2019-10-16
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70518-2364-0 | 70518236400 | 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2364-0) | 90 capsule | 2019-10-16 | 0000-00-00 | No | No | Current |
| 70518-2364-1 | 70518236401 | 60 CAPSULE in 1 BOTTLE, PLASTIC (70518-2364-1) | 60 capsule | 2021-07-15 | 0000-00-00 | No | No | Current |