| 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] |