OTEZLA
- Product NDC
- 59572-632
- 11-digit product format
- 595720632
- Labeler code
- 59572
- Product ID
- 59572-632_4b03ba80-afc7-4904-8c87-ef84b8fd25ea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- apremilast
- Dosage form
- KIT
- Route
- ORAL
- Labeler
- Celgene Corporation
- Application
- NDA205437
- Marketing category
- NDA
- Marketing start
- 2015-02-01
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 59572-632-55 | 59572063255 | 1 KIT in 1 BLISTER PACK (59572-632-55) | 1 kit | 2015-08-05 | 0000-00-00 | No | No | Current |