Dihydroergotamine Mesylate Nasal
- Product NDC
- 69097-740
- 11-digit product format
- 690970740
- Labeler code
- 69097
- Product ID
- 69097-740_c6908afb-ab07-4962-bb1c-5e671e1d2c54
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dihydroergotamine Mesylate Nasal
- Dosage form
- SPRAY, METERED
- Route
- NASAL
- Labeler
- Cipla USA Inc.
- Application
- ANDA212907
- Marketing category
- ANDA
- Marketing start
- 2020-12-11
- Marketing end
- 0000-00-00
- Substance
- DIHYDROERGOTAMINE MESYLATE
- Active strength
- 4 mg/mL
- Pharmacologic classes
- Ergotamine Derivative [EPC], Ergotamines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 69097-740-31 | 69097074031 | 1 VIAL in 1 KIT (69097-740-31) > 1 mL in 1 VIAL | 1 vial | 2020-12-11 | 0000-00-00 | No | No | Current |