Details for New Drug Application (NDA): 218663
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The generic ingredient in TERIFLUNOMIDE is teriflunomide. There are nineteen drug master file entries for this compound. Nineteen suppliers are listed for this compound. Additional details are available on the teriflunomide profile page.
Summary for 218663
| Tradename: | TERIFLUNOMIDE |
| Applicant: | Concord Biotech Ltd |
| 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 | 68254-5009 | 68254-5009-1 | 30 TABLET, FILM COATED in 1 BOTTLE (68254-5009-1) |
| TERIFLUNOMIDE | teriflunomide | TABLET;ORAL | 218663 | ANDA | CONCORD BIOTECH LIMITED | 68254-5010 | 68254-5010-1 | 30 TABLET, FILM COATED in 1 BOTTLE (68254-5010-1) |
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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