dimethyl fumarate
- Product NDC
- 0093-9218
- 11-digit product format
- 000939218
- Labeler code
- 0093
- Product ID
- 0093-9218_0b2673ca-4000-4697-ad2b-c36b7524e1f8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dimethyl fumarate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- TEVA PHARMACEUTICALS USA, INC.
- Application
- NDA204063
- Marketing category
- NDA
- Marketing start
- 2020-09-28
- Marketing end
- 2023-03-31
- Substance
- DIMETHYL FUMARATE
- Active strength
- 120 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0093-9218-41 | 00093921841 | 1 BOTTLE, PLASTIC in 1 CARTON (0093-9218-41) > 14 CAPSULE in 1 BOTTLE, PLASTIC | 2020-09-28 | 2023-03-31 | No | No | Current |