| Product NDC: | 35356-692 | 
| Proprietary Name: | meloxicam | 
| Non Proprietary Name: | meloxicam | 
| Active Ingredient(s): | 7.5 mg/1 & nbsp; meloxicam | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 35356-692 | 
| Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA077921 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20120214 | 
| Package NDC: | 35356-692-15 | 
| Package Description: | 15 TABLET in 1 BOTTLE (35356-692-15) | 
| NDC Code | 35356-692-15 | 
| Proprietary Name | meloxicam | 
| Package Description | 15 TABLET in 1 BOTTLE (35356-692-15) | 
| Product NDC | 35356-692 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | meloxicam | 
| Dosage Form Name | TABLET | 
| Route Name | ORAL | 
| Start Marketing Date | 20120214 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC | 
| Substance Name | MELOXICAM | 
| Strength Number | 7.5 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |