Pregabalin
- Product NDC
- 70518-2978
- 11-digit product format
- 705182978
- Labeler code
- 70518
- Product ID
- 70518-2978_d7ada92b-98ae-76ea-e053-2a95a90a75dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pregabalin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA209743
- Marketing category
- ANDA
- Marketing start
- 2020-12-28
- Marketing end
- 0000-00-00
- Substance
- PREGABALIN
- Active strength
- 300 mg/1
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2978-0 | 70518297800 | 60 CAPSULE in 1 BOTTLE, PLASTIC (70518-2978-0) | 60 capsule | 2020-12-28 | 0000-00-00 | No | No | Current |