Product NDC: | 0591-3525 |
Proprietary Name: | Lidocaine |
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: | 0591-3525 |
Labeler Name: | Watson Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA200675 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120823 |
Package NDC: | 0591-3525-30 |
Package Description: | 30 POUCH in 1 CARTON (0591-3525-30) > 1 PATCH in 1 POUCH (0591-3525-11) |
NDC Code | 0591-3525-30 |
Proprietary Name | Lidocaine |
Package Description | 30 POUCH in 1 CARTON (0591-3525-30) > 1 PATCH in 1 POUCH (0591-3525-11) |
Product NDC | 0591-3525 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Lidocaine |
Dosage Form Name | PATCH |
Route Name | CUTANEOUS |
Start Marketing Date | 20120823 |
Marketing Category Name | ANDA |
Labeler Name | Watson Laboratories, Inc. |
Substance Name | LIDOCAINE |
Strength Number | 700 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |