Details for New Drug Application (NDA): 218663
The generic ingredient in TERIFLUNOMIDE is teriflunomide. There is one drug master file entry for this compound. Seventeen suppliers are listed for this compound. Additional details are available on the teriflunomide profile page.
Summary for 218663
| Tradename: | TERIFLUNOMIDE |
| Applicant: | Neocubes Pharma |
| Ingredient: | teriflunomide |
| Patents: | 0 |
Pharmacology for NDA: 218663
| Mechanism of Action | Dihydroorotate Dehydrogenase Inhibitors |
Suppliers and Packaging for NDA: 218663
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| TERIFLUNOMIDE | teriflunomide | TABLET;ORAL | 218663 | ANDA | CONCORD BIOTECH LIMITED | 68254-5010 | 68254-5010-1 | 30 TABLET, FILM COATED in 1 BOTTLE (68254-5010-1) |
| TERIFLUNOMIDE | teriflunomide | TABLET;ORAL | 218663 | ANDA | CONCORD BIOTECH LIMITED | 68254-5013 | 68254-5013-1 | 30 TABLET, FILM COATED in 1 BOTTLE (68254-5013-1) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 7MG | ||||
| Approval Date: | Apr 7, 2025 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 14MG | ||||
| Approval Date: | Apr 7, 2025 | TE: | AB | RLD: | No | ||||
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