Pregabalin
- Product NDC
- 72606-006
- 11-digit product format
- 726060006
- Labeler code
- 72606
- Product ID
- 72606-006_f52fb718-9ad9-4e60-aec5-bbb97fe81a83
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- pregabalin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- CELLTRION USA, INC.
- Application
- ANDA212865
- Marketing category
- ANDA
- Marketing start
- 2020-03-31
- Marketing end
- 0000-00-00
- Substance
- PREGABALIN
- Active strength
- 75 mg/1
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 72606-006-01 | 72606000601 | 90 CAPSULE in 1 BOTTLE (72606-006-01) | 90 capsule | 2020-03-31 | 0000-00-00 | No | No | Current |