dimethyl fumarate
- Product NDC
- 24979-129
- 11-digit product format
- 249790129
- Labeler code
- 24979
- Product ID
- 24979-129_a21869da-1db2-42ca-9858-519c8bf094bb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dimethyl fumarate
- Dosage form
- KIT
- Labeler
- TWi Pharmaceuticals, Inc.
- Application
- ANDA210382
- Marketing category
- ANDA
- Marketing start
- 2020-12-01
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 24979-129-23 | 24979012923 | 1 KIT in 1 CARTON (24979-129-23) * 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC * 46 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC | 1 kit | 2020-12-01 | 0000-00-00 | No | No | Current |