| Product NDC: | 50436-1334 |
| Proprietary Name: | Lidocaine Hydrochloride |
| Non Proprietary Name: | Lidocaine |
| Active Ingredient(s): | 30 mg/g & nbsp; Lidocaine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50436-1334 |
| Labeler Name: | Unit Dose Services |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20130301 |
| Package NDC: | 50436-1334-1 |
| Package Description: | 30 g in 1 BOTTLE (50436-1334-1) |
| NDC Code | 50436-1334-1 |
| Proprietary Name | Lidocaine Hydrochloride |
| Package Description | 30 g in 1 BOTTLE (50436-1334-1) |
| Product NDC | 50436-1334 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lidocaine |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20130301 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Unit Dose Services |
| Substance Name | LIDOCAINE |
| Strength Number | 30 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |