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Lidocaine Hydrochloride - 49349-740-01 - (LIDOCAINE HYDROCHLORIDE ANHYDROUS)

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Drug Information of Lidocaine Hydrochloride

Product NDC: 49349-740
Proprietary Name: Lidocaine Hydrochloride
Non Proprietary Name: LIDOCAINE HYDROCHLORIDE ANHYDROUS
Active Ingredient(s): 10    mg/mL & nbsp;   LIDOCAINE HYDROCHLORIDE ANHYDROUS
Administration Route(s): INFILTRATION
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine Hydrochloride

Product NDC: 49349-740
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088299
Marketing Category: ANDA
Start Marketing Date: 20130612

Package Information of Lidocaine Hydrochloride

Package NDC: 49349-740-01
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (49349-740-01)

NDC Information of Lidocaine Hydrochloride

NDC Code 49349-740-01
Proprietary Name Lidocaine Hydrochloride
Package Description 50 mL in 1 VIAL, MULTI-DOSE (49349-740-01)
Product NDC 49349-740
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LIDOCAINE HYDROCHLORIDE ANHYDROUS
Dosage Form Name INJECTION, SOLUTION
Route Name INFILTRATION
Start Marketing Date 20130612
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name LIDOCAINE HYDROCHLORIDE ANHYDROUS
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE]

Complete Information of Lidocaine Hydrochloride


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