Product NDC: | 0603-1394 |
Proprietary Name: | Lidocaine Hydrochloride |
Non Proprietary Name: | Lidocaine Hydrochloride |
Active Ingredient(s): | 40 mg/mL & nbsp; Lidocaine Hydrochloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0603-1394 |
Labeler Name: | Qualitest Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040710 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070227 |
Package NDC: | 0603-1394-47 |
Package Description: | 50 mL in 1 BOTTLE (0603-1394-47) |
NDC Code | 0603-1394-47 |
Proprietary Name | Lidocaine Hydrochloride |
Package Description | 50 mL in 1 BOTTLE (0603-1394-47) |
Product NDC | 0603-1394 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Lidocaine Hydrochloride |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20070227 |
Marketing Category Name | ANDA |
Labeler Name | Qualitest Pharmaceuticals |
Substance Name | LIDOCAINE HYDROCHLORIDE |
Strength Number | 40 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |