Details for New Drug Application (NDA): 213703
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The generic ingredient in CANGRELOR is cangrelor. There are three drug master file entries for this compound. Two suppliers are listed for this compound. Additional details are available on the cangrelor profile page.
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | POWDER;INTRAVENOUS | Strength | 50MG/VIAL | ||||
| Approval Date: | Jun 4, 2026 | TE: | AP | RLD: | No | ||||
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