Dihydroergotamine Mesylate
- Product NDC
- 61990-0411
- 11-digit product format
- 619900411
- Labeler code
- 61990
- Product ID
- 61990-0411_d3973360-b84b-49a3-a17a-32529378b126
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dihydroergotamine Mesylate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Apollo Pharmaceuticals Inc.
- Application
- ANDA212046
- Marketing category
- ANDA
- Marketing start
- 2020-04-14
- Marketing end
- 0000-00-00
- Substance
- DIHYDROERGOTAMINE MESYLATE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Ergotamines [CS],Ergotamine Derivative [EPC]
- 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 |
|---|
| 61990-0411-1 | 61990041101 | 5 AMPULE in 1 CARTON (61990-0411-1) > 1 mL in 1 AMPULE (61990-0411-0) | 5 ampule | 2020-04-14 | 0000-00-00 | No | No | Current |
| 61990-0411-2 | 61990041102 | 10 AMPULE in 1 CARTON (61990-0411-2) > 1 mL in 1 AMPULE (61990-0411-0) | 10 ampule | 2020-04-14 | 0000-00-00 | No | No | Current |