Lidocaine - 0591-3525-30 - (Lidocaine)

Alphabetical Index


Drug Information of Lidocaine

Product NDC: 0591-3525
Proprietary Name: Lidocaine
Non Proprietary Name: Lidocaine
Active Ingredient(s): 700    mg/1 & nbsp;   Lidocaine
Administration Route(s): CUTANEOUS
Dosage Form(s): PATCH
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine

Product NDC: 0591-3525
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200675
Marketing Category: ANDA
Start Marketing Date: 20120823

Package Information of Lidocaine

Package NDC: 0591-3525-30
Package Description: 30 POUCH in 1 CARTON (0591-3525-30) > 1 PATCH in 1 POUCH (0591-3525-11)

NDC Information of Lidocaine

NDC Code 0591-3525-30
Proprietary Name Lidocaine
Package Description 30 POUCH in 1 CARTON (0591-3525-30) > 1 PATCH in 1 POUCH (0591-3525-11)
Product NDC 0591-3525
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine
Dosage Form Name PATCH
Route Name CUTANEOUS
Start Marketing Date 20120823
Marketing Category Name ANDA
Labeler Name Watson Laboratories, Inc.
Substance Name LIDOCAINE
Strength Number 700
Strength Unit mg/1
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE]

Complete Information of Lidocaine


General Information