Product NDC: | 54868-5411 |
Proprietary Name: | Cilostazol |
Non Proprietary Name: | Cilostazol |
Active Ingredient(s): | 100 mg/1 & nbsp; Cilostazol |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-5411 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077022 |
Marketing Category: | ANDA |
Start Marketing Date: | 20050909 |
Package NDC: | 54868-5411-0 |
Package Description: | 60 TABLET in 1 BOTTLE, PLASTIC (54868-5411-0) |
NDC Code | 54868-5411-0 |
Proprietary Name | Cilostazol |
Package Description | 60 TABLET in 1 BOTTLE, PLASTIC (54868-5411-0) |
Product NDC | 54868-5411 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Cilostazol |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20050909 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | CILOSTAZOL |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Phosphodiesterase 3 Inhibitor [EPC],Phosphodiesterase 3 Inhibitors [MoA] |