Details for New Drug Application (NDA): 205122
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The generic ingredient in QUDEXY XR is topiramate. There are twenty-six drug master file entries for this compound. Forty-eight suppliers are listed for this compound. Additional details are available on the topiramate profile page.
Summary for 205122
| Tradename: | QUDEXY XR |
| Applicant: | Upsher Smith Labs |
| Ingredient: | topiramate |
| Patents: | 5 |
Pharmacology for NDA: 205122
| Mechanism of Action | Cytochrome P450 2C19 Inhibitors Cytochrome P450 3A4 Inducers |
| Physiological Effect | Decreased Central Nervous System Disorganized Electrical Activity |
Suppliers and Packaging for NDA: 205122
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| QUDEXY XR | topiramate | CAPSULE, EXTENDED RELEASE;ORAL | 205122 | NDA | Upsher-Smith Laboratories, LLC | 0245-1071 | 0245-1071-30 | 1 BOTTLE in 1 CARTON (0245-1071-30) / 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE |
| QUDEXY XR | topiramate | CAPSULE, EXTENDED RELEASE;ORAL | 205122 | NDA | Upsher-Smith Laboratories, LLC | 0245-1071 | 0245-1071-90 | 1 BOTTLE in 1 CARTON (0245-1071-90) / 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | 25MG | ||||
| Approval Date: | Mar 11, 2014 | TE: | AB2 | RLD: | Yes | ||||
| Patent: | 10,363,224 | Patent Expiration: | Mar 19, 2033 | Product Flag? | Substance Flag? | Delist Request? | |||
| Patented Use: | TREATMENT OF SEIZURES | ||||||||
| Patent: | 8,652,527 | Patent Expiration: | Mar 19, 2033 | Product Flag? | Y | Substance Flag? | Delist Request? | ||
| Patent: | 8,889,190 | Patent Expiration: | Mar 19, 2033 | Product Flag? | Y | Substance Flag? | Delist Request? | ||
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