| Product NDC: | 49999-419 | 
| Proprietary Name: | LIDODERM | 
| Non Proprietary Name: | LIDODERM | 
| Active Ingredient(s): | 700 mg/1 & nbsp; LIDODERM | 
| Administration Route(s): | CUTANEOUS | 
| Dosage Form(s): | PATCH | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 49999-419 | 
| Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | NDA020612 | 
| Marketing Category: | NDA | 
| Start Marketing Date: | 20111201 | 
| Package NDC: | 49999-419-30 | 
| Package Description: | 30 POUCH in 1 CARTON (49999-419-30) > 1 PATCH in 1 POUCH | 
| NDC Code | 49999-419-30 | 
| Proprietary Name | LIDODERM | 
| Package Description | 30 POUCH in 1 CARTON (49999-419-30) > 1 PATCH in 1 POUCH | 
| Product NDC | 49999-419 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | LIDODERM | 
| Dosage Form Name | PATCH | 
| Route Name | CUTANEOUS | 
| Start Marketing Date | 20111201 | 
| Marketing Category Name | NDA | 
| Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC | 
| Substance Name | LIDOCAINE | 
| Strength Number | 700 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |