Details for New Drug Application (NDA): 200562
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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 200562
| Tradename: | CELECOXIB |
| Applicant: | Watson Labs Inc |
| Ingredient: | celecoxib |
| Patents: | 0 |
Pharmacology for NDA: 200562
| Mechanism of Action | Cyclooxygenase Inhibitors |
Medical Subject Heading (MeSH) Categories for 200562
Suppliers and Packaging for NDA: 200562
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| CELECOXIB | celecoxib | CAPSULE;ORAL | 200562 | ANDA | Actavis Pharma, Inc. | 0591-3982 | 0591-3982-60 | 60 CAPSULE in 1 BOTTLE (0591-3982-60) |
| CELECOXIB | celecoxib | CAPSULE;ORAL | 200562 | ANDA | Actavis Pharma, Inc. | 0591-3983 | 0591-3983-01 | 100 CAPSULE in 1 BOTTLE (0591-3983-01) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 50MG | ||||
| Approval Date: | Feb 11, 2015 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 100MG | ||||
| Approval Date: | Feb 11, 2015 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 200MG | ||||
| Approval Date: | Feb 11, 2015 | TE: | AB | RLD: | No | ||||
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