Product NDC: | 55390-555 |
Proprietary Name: | Dipyridamole |
Non Proprietary Name: | Dipyridamole |
Active Ingredient(s): | 5 mg/mL & nbsp; Dipyridamole |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55390-555 |
Labeler Name: | Bedford Laboratories |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074939 |
Marketing Category: | ANDA |
Start Marketing Date: | 19980601 |
Package NDC: | 55390-555-10 |
Package Description: | 10 VIAL in 1 BOX (55390-555-10) > 2 mL in 1 VIAL |
NDC Code | 55390-555-10 |
Proprietary Name | Dipyridamole |
Package Description | 10 VIAL in 1 BOX (55390-555-10) > 2 mL in 1 VIAL |
Product NDC | 55390-555 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Dipyridamole |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19980601 |
Marketing Category Name | ANDA |
Labeler Name | Bedford Laboratories |
Substance Name | DIPYRIDAMOLE |
Strength Number | 5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC] |