Product NDC: | 64896-681 |
Proprietary Name: | ZOMIG |
Non Proprietary Name: | Zolmitriptan |
Active Ingredient(s): | 5 mg/1 & nbsp; Zolmitriptan |
Administration Route(s): | NASAL |
Dosage Form(s): | SPRAY, METERED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64896-681 |
Labeler Name: | Impax Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021450 |
Marketing Category: | NDA |
Start Marketing Date: | 20120702 |
Package NDC: | 64896-681-51 |
Package Description: | 6 BOTTLE, SPRAY in 1 CARTON (64896-681-51) > 1 SPRAY, METERED in 1 BOTTLE, SPRAY |
NDC Code | 64896-681-51 |
Proprietary Name | ZOMIG |
Package Description | 6 BOTTLE, SPRAY in 1 CARTON (64896-681-51) > 1 SPRAY, METERED in 1 BOTTLE, SPRAY |
Product NDC | 64896-681 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Zolmitriptan |
Dosage Form Name | SPRAY, METERED |
Route Name | NASAL |
Start Marketing Date | 20120702 |
Marketing Category Name | NDA |
Labeler Name | Impax Laboratories, Inc. |
Substance Name | ZOLMITRIPTAN |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |