NDC Code | 68083-412-10 |
Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (68083-412-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE |
Product NDC | 68083-412 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Cangrelor |
Non-Proprietary Name | Cangrelor |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Usage | INTRAVENOUS |
Start Marketing Date | 20250811 |
Marketing Category Name | ANDA |
Application Number | ANDA213551 |
Manufacturer | Gland Pharma Limited |
Substance Name | CANGRELOR |
Strength | 50 |
Strength Unit | mg/1 |
Pharmacy Classes | Decreased Platelet Aggregation [PE], P2Y12 Platelet Inhibitor [EPC], P2Y12 Receptor Antagonists [MoA] |