Product NDC: | 54569-4671 |
Proprietary Name: | CELEBREX |
Non Proprietary Name: | Celecoxib |
Active Ingredient(s): | 100 mg/1 & nbsp; Celecoxib |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54569-4671 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020998 |
Marketing Category: | NDA |
Start Marketing Date: | 19990125 |
Package NDC: | 54569-4671-0 |
Package Description: | 60 CAPSULE in 1 BOTTLE (54569-4671-0) |
NDC Code | 54569-4671-0 |
Proprietary Name | CELEBREX |
Package Description | 60 CAPSULE in 1 BOTTLE (54569-4671-0) |
Product NDC | 54569-4671 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Celecoxib |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 19990125 |
Marketing Category Name | NDA |
Labeler Name | A-S Medication Solutions LLC |
Substance Name | CELECOXIB |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |