Lidocaine - 54868-4195-0 - (Lidocaine Hydrochloride)

Alphabetical Index


Drug Information of Lidocaine

Product NDC: 54868-4195
Proprietary Name: Lidocaine
Non Proprietary Name: Lidocaine Hydrochloride
Active Ingredient(s): 20    mg/mL & nbsp;   Lidocaine Hydrochloride
Administration Route(s): TOPICAL
Dosage Form(s): JELLY
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine

Product NDC: 54868-4195
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040433
Marketing Category: ANDA
Start Marketing Date: 20000601

Package Information of Lidocaine

Package NDC: 54868-4195-0
Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON (54868-4195-0) > 30 mL in 1 TUBE, WITH APPLICATOR

NDC Information of Lidocaine

NDC Code 54868-4195-0
Proprietary Name Lidocaine
Package Description 1 TUBE, WITH APPLICATOR in 1 CARTON (54868-4195-0) > 30 mL in 1 TUBE, WITH APPLICATOR
Product NDC 54868-4195
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine Hydrochloride
Dosage Form Name JELLY
Route Name TOPICAL
Start Marketing Date 20000601
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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


General Information