Product NDC: | 49349-872 |
Proprietary Name: | CELEBREX |
Non Proprietary Name: | CELECOXIB |
Active Ingredient(s): | 200 mg/1 & nbsp; CELECOXIB |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49349-872 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020998 |
Marketing Category: | NDA |
Start Marketing Date: | 20130220 |
Package NDC: | 49349-872-11 |
Package Description: | 7 CAPSULE in 1 VIAL (49349-872-11) |
NDC Code | 49349-872-11 |
Proprietary Name | CELEBREX |
Package Description | 7 CAPSULE in 1 VIAL (49349-872-11) |
Product NDC | 49349-872 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CELECOXIB |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20130220 |
Marketing Category Name | NDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | CELECOXIB |
Strength Number | 200 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |