Details for New Drug Application (NDA): 202666
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The generic ingredient in DEXLANSOPRAZOLE is dexlansoprazole. There are seventeen drug master file entries for this compound. Eleven suppliers are listed for this compound. Additional details are available on the dexlansoprazole profile page.
Summary for 202666
| Tradename: | DEXLANSOPRAZOLE |
| Applicant: | Twi Pharms |
| Ingredient: | dexlansoprazole |
| Patents: | 0 |
Pharmacology for NDA: 202666
| Mechanism of Action | Proton Pump Inhibitors |
Medical Subject Heading (MeSH) Categories for 202666
Suppliers and Packaging for NDA: 202666
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| DEXLANSOPRAZOLE | dexlansoprazole | CAPSULE, DELAYED RELEASE;ORAL | 202666 | ANDA | Upsher-Smith Laboratories, LLC | 24979-001 | 24979-001-06 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (24979-001-06) |
| DEXLANSOPRAZOLE | dexlansoprazole | CAPSULE, DELAYED RELEASE;ORAL | 202666 | ANDA | Upsher-Smith Laboratories, LLC | 24979-001 | 24979-001-07 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (24979-001-07) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, DELAYED RELEASE;ORAL | Strength | 30MG | ||||
| Approval Date: | Sep 16, 2022 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, DELAYED RELEASE;ORAL | Strength | 60MG | ||||
| Approval Date: | Sep 16, 2022 | TE: | AB | RLD: | No | ||||
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