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Lidocaine Hydrochloride - 54569-1285-0 - (Lidocaine Hydrochloride)

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Drug Information of Lidocaine Hydrochloride

Product NDC: 54569-1285
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: 54569-1285
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040708
Marketing Category: ANDA
Start Marketing Date: 20070227

Package Information of Lidocaine Hydrochloride

Package NDC: 54569-1285-0
Package Description: 100 mL in 1 BOTTLE (54569-1285-0)

NDC Information of Lidocaine Hydrochloride

NDC Code 54569-1285-0
Proprietary Name Lidocaine Hydrochloride
Package Description 100 mL in 1 BOTTLE (54569-1285-0)
Product NDC 54569-1285
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 A-S Medication Solutions LLC
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


General Information