| Product NDC: | 49999-383 | 
| 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: | 49999-383 | 
| Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | NDA020998 | 
| Marketing Category: | NDA | 
| Start Marketing Date: | 20111122 | 
| Package NDC: | 49999-383-10 | 
| Package Description: | 10 CAPSULE in 1 BOTTLE (49999-383-10) | 
| NDC Code | 49999-383-10 | 
| Proprietary Name | CELEBREX | 
| Package Description | 10 CAPSULE in 1 BOTTLE (49999-383-10) | 
| Product NDC | 49999-383 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Celecoxib | 
| Dosage Form Name | CAPSULE | 
| Route Name | ORAL | 
| Start Marketing Date | 20111122 | 
| Marketing Category Name | NDA | 
| Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products 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] |