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Lidocaine Hydrochloride and Epinephrine - 52125-612-01 - (LIDOCAINE HYDROCHLORIDE ANHYDROUS and EPINEPHRINE)

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Drug Information of Lidocaine Hydrochloride and Epinephrine

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)

Labeler Information of Lidocaine Hydrochloride and Epinephrine

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 Information of Lidocaine Hydrochloride and Epinephrine

Package NDC: 52125-612-01
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (52125-612-01)

NDC Information of Lidocaine Hydrochloride and Epinephrine

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]

Complete Information of Lidocaine Hydrochloride and Epinephrine


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