Frova - 35356-169-09 - (Frovatriptan succinate)

Alphabetical Index


Drug Information of Frova

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)

Labeler Information of Frova

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 Information of Frova

Package NDC: 35356-169-09
Package Description: 9 TABLET, FILM COATED in 1 BLISTER PACK (35356-169-09)

NDC Information of Frova

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]

Complete Information of Frova


General Information