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Dihydroergotamine Mesylate
Dihydroergotamine Mesylate - 68682-357-10 - (dihydroergotamine mesylate)
Drug Information of Dihydroergotamine Mesylate
| Product NDC: | 68682-357 |
| Proprietary Name: | Dihydroergotamine Mesylate |
| Non Proprietary Name: | dihydroergotamine mesylate |
| Active Ingredient(s): | 4 mg/mL & nbsp; dihydroergotamine mesylate |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dihydroergotamine Mesylate
| Product NDC: | 68682-357 |
| Labeler Name: | Oceanside Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020148 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20130318 |
Package Information of Dihydroergotamine Mesylate
| Package NDC: | 68682-357-10 |
| Package Description: | 8 VIAL in 1 KIT (68682-357-10) > 1 mL in 1 VIAL |
NDC Information of Dihydroergotamine Mesylate
| NDC Code | 68682-357-10 |
| Proprietary Name | Dihydroergotamine Mesylate |
| Package Description | 8 VIAL in 1 KIT (68682-357-10) > 1 mL in 1 VIAL |
| Product NDC | 68682-357 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | dihydroergotamine mesylate |
| Dosage Form Name | SPRAY |
| Route Name | NASAL |
| Start Marketing Date | 20130318 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Oceanside Pharmaceuticals |
| Substance Name | DIHYDROERGOTAMINE MESYLATE |
| Strength Number | 4 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Ergotamine Derivative [EPC],Ergotamines [Chemical/Ingredient] |
