Product NDC: | 55154-1337 |
Proprietary Name: | DIPYRIDAMOLE |
Non Proprietary Name: | DIPYRIDAMOLE |
Active Ingredient(s): | 75 mg/1 & nbsp; DIPYRIDAMOLE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-1337 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040733 |
Marketing Category: | ANDA |
Start Marketing Date: | 20081030 |
Package NDC: | 55154-1337-0 |
Package Description: | 10 BLISTER PACK in 1 BAG (55154-1337-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Code | 55154-1337-0 |
Proprietary Name | DIPYRIDAMOLE |
Package Description | 10 BLISTER PACK in 1 BAG (55154-1337-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK |
Product NDC | 55154-1337 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | DIPYRIDAMOLE |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20081030 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | DIPYRIDAMOLE |
Strength Number | 75 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC] |