| 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] |