Product NDC: | 35356-254 |
Proprietary Name: | IMITREX |
Non Proprietary Name: | sumatriptan succinate |
Active Ingredient(s): | 100 mg/1 & nbsp; sumatriptan succinate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 35356-254 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020132 |
Marketing Category: | NDA |
Start Marketing Date: | 20120328 |
Package NDC: | 35356-254-09 |
Package Description: | 9 TABLET, FILM COATED in 1 BLISTER PACK (35356-254-09) |
NDC Code | 35356-254-09 |
Proprietary Name | IMITREX |
Package Description | 9 TABLET, FILM COATED in 1 BLISTER PACK (35356-254-09) |
Product NDC | 35356-254 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | sumatriptan succinate |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20120328 |
Marketing Category Name | NDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | SUMATRIPTAN SUCCINATE |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |