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] |