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Lidocaine Hydrochloride - 0409-1323-05 - (LIDOCAINE HYDROCHLORIDE)

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Drug Information of Lidocaine Hydrochloride

Product NDC: 0409-1323
Proprietary Name: Lidocaine Hydrochloride
Non Proprietary Name: LIDOCAINE HYDROCHLORIDE
Active Ingredient(s): 20    mg/mL & nbsp;   LIDOCAINE HYDROCHLORIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine Hydrochloride

Product NDC: 0409-1323
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040302
Marketing Category: ANDA
Start Marketing Date: 20101129

Package Information of Lidocaine Hydrochloride

Package NDC: 0409-1323-05
Package Description: 10 CARTON in 1 CONTAINER (0409-1323-05) > 1 SYRINGE, PLASTIC in 1 CARTON > 5 mL in 1 SYRINGE, PLASTIC

NDC Information of Lidocaine Hydrochloride

NDC Code 0409-1323-05
Proprietary Name Lidocaine Hydrochloride
Package Description 10 CARTON in 1 CONTAINER (0409-1323-05) > 1 SYRINGE, PLASTIC in 1 CARTON > 5 mL in 1 SYRINGE, PLASTIC
Product NDC 0409-1323
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LIDOCAINE HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20101129
Marketing Category Name ANDA
Labeler Name Hospira, 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]

Complete Information of Lidocaine Hydrochloride


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