Product NDC: | 63629-4761 |
Proprietary Name: | LIDODERM |
Non Proprietary Name: | lidocaine |
Active Ingredient(s): | 700 mg/1 & nbsp; lidocaine |
Administration Route(s): | CUTANEOUS |
Dosage Form(s): | PATCH |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63629-4761 |
Labeler Name: | Bryant Ranch Prepack |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020612 |
Marketing Category: | NDA |
Start Marketing Date: | 19990320 |
Package NDC: | 63629-4761-1 |
Package Description: | 1 PATCH in 1 BOTTLE (63629-4761-1) |
NDC Code | 63629-4761-1 |
Proprietary Name | LIDODERM |
Package Description | 1 PATCH in 1 BOTTLE (63629-4761-1) |
Product NDC | 63629-4761 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | lidocaine |
Dosage Form Name | PATCH |
Route Name | CUTANEOUS |
Start Marketing Date | 19990320 |
Marketing Category Name | NDA |
Labeler Name | Bryant Ranch Prepack |
Substance Name | LIDOCAINE |
Strength Number | 700 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |