dihydroergotamine mesylate
- Product NDC
- 0574-0851
- 11-digit product format
- 005740851
- Labeler code
- 0574
- Product ID
- 0574-0851_e8fd3444-ae35-4f0d-bcd1-80588d0f4f3f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dihydroergotamine mesylate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Paddock Laboratories, LLC.
- Application
- ANDA040475
- Marketing category
- ANDA
- Marketing start
- 2020-05-18
- Marketing end
- 2021-09-30
- Substance
- DIHYDROERGOTAMINE MESYLATE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Ergotamines [CS],Ergotamine Derivative [EPC]
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0574-0851-05 | 00574085105 | 5 AMPULE in 1 CARTON (0574-0851-05) > 1 mL in 1 AMPULE | 5 ampule | 2020-05-18 | 2021-09-30 | No | No | Current |
| 0574-0851-10 | 00574085110 | 10 AMPULE in 1 CARTON (0574-0851-10) > 1 mL in 1 AMPULE | 10 ampule | 2020-08-05 | 2021-08-31 | No | No | Current |