Product NDC: | 52125-612 |
Proprietary Name: | Lidocaine Hydrochloride and Epinephrine |
Non Proprietary Name: | LIDOCAINE HYDROCHLORIDE ANHYDROUS and EPINEPHRINE |
Active Ingredient(s): | 10; 10 ug/mL; mg/mL & nbsp; LIDOCAINE HYDROCHLORIDE ANHYDROUS and EPINEPHRINE |
Administration Route(s): | INFILTRATION |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52125-612 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA089644 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130705 |
Package NDC: | 52125-612-01 |
Package Description: | 30 mL in 1 VIAL, MULTI-DOSE (52125-612-01) |
NDC Code | 52125-612-01 |
Proprietary Name | Lidocaine Hydrochloride and Epinephrine |
Package Description | 30 mL in 1 VIAL, MULTI-DOSE (52125-612-01) |
Product NDC | 52125-612 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | LIDOCAINE HYDROCHLORIDE ANHYDROUS and EPINEPHRINE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INFILTRATION |
Start Marketing Date | 20130705 |
Marketing Category Name | ANDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | EPINEPHRINE; LIDOCAINE HYDROCHLORIDE ANHYDROUS |
Strength Number | 10; 10 |
Strength Unit | ug/mL; mg/mL |
Pharmaceutical Classes | Adrenergic alpha-Agonists [MoA],Adrenergic beta-Agonists [MoA],alpha-Adrenergic Agonist [EPC],beta-Adrenergic Agonist [EPC],Catecholamine [EPC],Catecholamines [Chemical/Ingredient],Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |