Product NDC: | 35356-169 |
Proprietary Name: | Frova |
Non Proprietary Name: | Frovatriptan succinate |
Active Ingredient(s): | 2.5 mg/1 & nbsp; Frovatriptan succinate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 35356-169 |
Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021006 |
Marketing Category: | NDA |
Start Marketing Date: | 20100818 |
Package NDC: | 35356-169-09 |
Package Description: | 9 TABLET, FILM COATED in 1 BLISTER PACK (35356-169-09) |
NDC Code | 35356-169-09 |
Proprietary Name | Frova |
Package Description | 9 TABLET, FILM COATED in 1 BLISTER PACK (35356-169-09) |
Product NDC | 35356-169 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Frovatriptan succinate |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20100818 |
Marketing Category Name | NDA |
Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
Substance Name | FROVATRIPTAN SUCCINATE |
Strength Number | 2.5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |