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LIDODERM
LIDODERM - 50436-1331-1 - (lidocaine)
Drug Information of LIDODERM
| Product NDC: | 50436-1331 |
| 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) |
Labeler Information of LIDODERM
| Product NDC: | 50436-1331 |
| Labeler Name: | Unit Dose Services |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020612 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19990320 |
Package Information of LIDODERM
| Package NDC: | 50436-1331-1 |
| Package Description: | 30 PATCH in 1 PATCH (50436-1331-1) |
NDC Information of LIDODERM
| NDC Code | 50436-1331-1 |
| Proprietary Name | LIDODERM |
| Package Description | 30 PATCH in 1 PATCH (50436-1331-1) |
| Product NDC | 50436-1331 |
| 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 | Unit Dose Services |
| Substance Name | LIDOCAINE |
| Strength Number | 700 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |
