Lidocaine - 17478-711-30 - (Lidocaine Hydrochloride)

Alphabetical Index


Drug Information of Lidocaine

Product NDC: 17478-711
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: 17478-711
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040433
Marketing Category: ANDA
Start Marketing Date: 20030801

Package Information of Lidocaine

Package NDC: 17478-711-30
Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON (17478-711-30) > 30 mL in 1 TUBE, WITH APPLICATOR

NDC Information of Lidocaine

NDC Code 17478-711-30
Proprietary Name Lidocaine
Package Description 1 TUBE, WITH APPLICATOR in 1 CARTON (17478-711-30) > 30 mL in 1 TUBE, WITH APPLICATOR
Product NDC 17478-711
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine Hydrochloride
Dosage Form Name JELLY
Route Name TOPICAL
Start Marketing Date 20030801
Marketing Category Name ANDA
Labeler Name Akorn, 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