Product NDC: | 0054-8500 |
Proprietary Name: | Lidocaine Viscous |
Non Proprietary Name: | Lidocaine Hydrochloride |
Active Ingredient(s): | 20 mg/mL & nbsp; Lidocaine Hydrochloride |
Administration Route(s): | ORAL; TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0054-8500 |
Labeler Name: | Roxane Laboratories,Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA088802 |
Marketing Category: | ANDA |
Start Marketing Date: | 19850426 |
Package NDC: | 0054-8500-16 |
Package Description: | 10 CUP, UNIT-DOSE in 1 CARTON (0054-8500-16) > 20 mL in 1 CUP, UNIT-DOSE |
NDC Code | 0054-8500-16 |
Proprietary Name | Lidocaine Viscous |
Package Description | 10 CUP, UNIT-DOSE in 1 CARTON (0054-8500-16) > 20 mL in 1 CUP, UNIT-DOSE |
Product NDC | 0054-8500 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Lidocaine Hydrochloride |
Dosage Form Name | SOLUTION |
Route Name | ORAL; TOPICAL |
Start Marketing Date | 19850426 |
Marketing Category Name | ANDA |
Labeler Name | Roxane Laboratories,Inc |
Substance Name | LIDOCAINE HYDROCHLORIDE |
Strength Number | 20 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |