Details for New Drug Application (NDA): 208833
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The generic ingredient in CELECOXIB is celecoxib. There are twenty-six drug master file entries for this compound. Sixty-five suppliers are listed for this compound. Additional details are available on the celecoxib profile page.
Summary for 208833
| Tradename: | CELECOXIB |
| Applicant: | Amneal Pharms |
| Ingredient: | celecoxib |
| Patents: | 0 |
Pharmacology for NDA: 208833
| Mechanism of Action | Cyclooxygenase Inhibitors |
Medical Subject Heading (MeSH) Categories for 208833
Suppliers and Packaging for NDA: 208833
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| CELECOXIB | celecoxib | CAPSULE;ORAL | 208833 | ANDA | Amneal Pharmaceuticals LLC | 65162-817 | 65162-817-06 | 60 CAPSULE in 1 BOTTLE (65162-817-06) |
| CELECOXIB | celecoxib | CAPSULE;ORAL | 208833 | ANDA | Amneal Pharmaceuticals LLC | 65162-818 | 65162-818-10 | 100 CAPSULE in 1 BOTTLE (65162-818-10) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | CAPSULE;ORAL | Strength | 50MG | ||||
| Approval Date: | May 31, 2018 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | CAPSULE;ORAL | Strength | 100MG | ||||
| Approval Date: | May 31, 2018 | TE: | RLD: | No | |||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | CAPSULE;ORAL | Strength | 200MG | ||||
| Approval Date: | May 31, 2018 | TE: | RLD: | No | |||||
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