Product NDC: | 29336-305 |
Proprietary Name: | TAMBOCOR |
Non Proprietary Name: | flecainide acetate |
Active Ingredient(s): | 50 mg/1 & nbsp; flecainide acetate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 29336-305 |
Labeler Name: | Graceway Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018830 |
Marketing Category: | NDA |
Start Marketing Date: | 20070401 |
Package NDC: | 29336-305-10 |
Package Description: | 100 TABLET in 1 BOTTLE (29336-305-10) |
NDC Code | 29336-305-10 |
Proprietary Name | TAMBOCOR |
Package Description | 100 TABLET in 1 BOTTLE (29336-305-10) |
Product NDC | 29336-305 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | flecainide acetate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20070401 |
Marketing Category Name | NDA |
Labeler Name | Graceway Pharmaceuticals, LLC |
Substance Name | FLECAINIDE ACETATE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Antiarrhythmic [EPC] |