Lidocaine - 51672-3020-2 - (Lidocaine)

Alphabetical Index


Drug Information of Lidocaine

Product NDC: 51672-3020
Proprietary Name: Lidocaine
Non Proprietary Name: Lidocaine
Active Ingredient(s): 50    mg/g & nbsp;   Lidocaine
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine

Product NDC: 51672-3020
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086724
Marketing Category: ANDA
Start Marketing Date: 20130325

Package Information of Lidocaine

Package NDC: 51672-3020-2
Package Description: 1 TUBE in 1 CARTON (51672-3020-2) > 30 g in 1 TUBE

NDC Information of Lidocaine

NDC Code 51672-3020-2
Proprietary Name Lidocaine
Package Description 1 TUBE in 1 CARTON (51672-3020-2) > 30 g in 1 TUBE
Product NDC 51672-3020
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20130325
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name LIDOCAINE
Strength Number 50
Strength Unit mg/g
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE]

Complete Information of Lidocaine


General Information