Product NDC: | 21695-656 |
Proprietary Name: | Aggrenox |
Non Proprietary Name: | aspirin and dipyridamole |
Active Ingredient(s): | 25; 200 mg/1; mg/1 & nbsp; aspirin and dipyridamole |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-656 |
Labeler Name: | Rebel Distributors Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020884 |
Marketing Category: | NDA |
Start Marketing Date: | 19991219 |
Package NDC: | 21695-656-60 |
Package Description: | 60 CAPSULE in 1 BOTTLE (21695-656-60) |
NDC Code | 21695-656-60 |
Proprietary Name | Aggrenox |
Package Description | 60 CAPSULE in 1 BOTTLE (21695-656-60) |
Product NDC | 21695-656 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | aspirin and dipyridamole |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 19991219 |
Marketing Category Name | NDA |
Labeler Name | Rebel Distributors Corp. |
Substance Name | ASPIRIN; DIPYRIDAMOLE |
Strength Number | 25; 200 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC],Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC] |