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Lidocaine Hydrochloride - 0603-1393-64 - (Lidocaine Hydrochloride)

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Drug Information of Lidocaine Hydrochloride

Product NDC: 0603-1393
Proprietary Name: Lidocaine Hydrochloride
Non Proprietary Name: Lidocaine Hydrochloride
Active Ingredient(s): 20    mg/mL & nbsp;   Lidocaine Hydrochloride
Administration Route(s): OROPHARYNGEAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine Hydrochloride

Product NDC: 0603-1393
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040708
Marketing Category: ANDA
Start Marketing Date: 20070227

Package Information of Lidocaine Hydrochloride

Package NDC: 0603-1393-64
Package Description: 100 mL in 1 BOTTLE (0603-1393-64)

NDC Information of Lidocaine Hydrochloride

NDC Code 0603-1393-64
Proprietary Name Lidocaine Hydrochloride
Package Description 100 mL in 1 BOTTLE (0603-1393-64)
Product NDC 0603-1393
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine Hydrochloride
Dosage Form Name SOLUTION
Route Name OROPHARYNGEAL
Start Marketing Date 20070227
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
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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