Product NDC: | 35356-936 |
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: | 35356-936 |
Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20130301 |
Package NDC: | 35356-936-30 |
Package Description: | 1 TUBE in 1 CARTON (35356-936-30) > 28.5 g in 1 TUBE |
NDC Code | 35356-936-30 |
Proprietary Name | Lidocaine Hydrochloride |
Package Description | 1 TUBE in 1 CARTON (35356-936-30) > 28.5 g in 1 TUBE |
Product NDC | 35356-936 |
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 | Lake Erie Medical DBA Quality Care Products LLC |
Substance Name | LIDOCAINE |
Strength Number | 30 |
Strength Unit | mg/g |
Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |