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Dipyridamole
Dipyridamole - 0641-2569-44 - (Dipyridamole)
Drug Information of Dipyridamole
| Product NDC: | 0641-2569 |
| 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) |
Labeler Information of Dipyridamole
| Product NDC: | 0641-2569 |
| Labeler Name: | West-ward Pharmaceutical Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074521 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19961018 |
Package Information of Dipyridamole
| Package NDC: | 0641-2569-44 |
| Package Description: | 5 VIAL in 1 CARTON (0641-2569-44) > 10 mL in 1 VIAL (0641-2569-41) |
NDC Information of Dipyridamole
| NDC Code | 0641-2569-44 |
| Proprietary Name | Dipyridamole |
| Package Description | 5 VIAL in 1 CARTON (0641-2569-44) > 10 mL in 1 VIAL (0641-2569-41) |
| Product NDC | 0641-2569 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dipyridamole |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19961018 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp. |
| Substance Name | DIPYRIDAMOLE |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC] |
