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Lidocaine Hydrochloride - 0409-4282-01 - (LIDOCAINE HYDROCHLORIDE ANHYDROUS)

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Drug Information of Lidocaine Hydrochloride

Product NDC: 0409-4282
Proprietary Name: Lidocaine Hydrochloride
Non Proprietary Name: LIDOCAINE HYDROCHLORIDE ANHYDROUS
Active Ingredient(s): 20    mg/mL & nbsp;   LIDOCAINE HYDROCHLORIDE ANHYDROUS
Administration Route(s): EPIDURAL; INFILTRATION
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine Hydrochloride

Product NDC: 0409-4282
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088294
Marketing Category: ANDA
Start Marketing Date: 20100330

Package Information of Lidocaine Hydrochloride

Package NDC: 0409-4282-01
Package Description: 5 TRAY in 1 PACKAGE (0409-4282-01) > 5 AMPULE in 1 TRAY > 2 mL in 1 AMPULE

NDC Information of Lidocaine Hydrochloride

NDC Code 0409-4282-01
Proprietary Name Lidocaine Hydrochloride
Package Description 5 TRAY in 1 PACKAGE (0409-4282-01) > 5 AMPULE in 1 TRAY > 2 mL in 1 AMPULE
Product NDC 0409-4282
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LIDOCAINE HYDROCHLORIDE ANHYDROUS
Dosage Form Name INJECTION, SOLUTION
Route Name EPIDURAL; INFILTRATION
Start Marketing Date 20100330
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name LIDOCAINE HYDROCHLORIDE ANHYDROUS
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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