Details for New Drug Application (NDA): 214275
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The generic ingredient in UPTRAVI is selexipag. There are two drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the selexipag profile page.
Pharmacology for NDA: 214275
| Mechanism of Action | Prostacyclin Receptor Agonists |
Suppliers and Packaging for NDA: 214275
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| UPTRAVI | selexipag | POWDER;INTRAVENOUS | 214275 | NDA | Actelion Pharmaceuticals US, Inc. | 66215-718 | 66215-718-01 | 1 VIAL, SINGLE-DOSE in 1 CARTON (66215-718-01) / 10 mL in 1 VIAL, SINGLE-DOSE |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | POWDER;INTRAVENOUS | Strength | 1.8MG/VIAL | ||||
| Approval Date: | Jul 29, 2021 | TE: | RLD: | Yes | |||||
| Patent: | 7,205,302*PED | Patent Expiration: | Apr 30, 2027 | Product Flag? | Substance Flag? | Delist Request? | Y | ||
| Patent: | 8,791,122*PED | Patent Expiration: | Feb 1, 2031 | Product Flag? | Substance Flag? | Delist Request? | Y | ||
| Patent: | 9,173,881*PED | Patent Expiration: | Feb 12, 2030 | Product Flag? | Substance Flag? | Delist Request? | Y | ||
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