LIDODERM - 63629-4761-1 - (lidocaine)

Alphabetical Index


Drug Information of LIDODERM

Product NDC: 63629-4761
Proprietary Name: LIDODERM
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 LIDODERM

Product NDC: 63629-4761
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020612
Marketing Category: NDA
Start Marketing Date: 19990320

Package Information of LIDODERM

Package NDC: 63629-4761-1
Package Description: 1 PATCH in 1 BOTTLE (63629-4761-1)

NDC Information of LIDODERM

NDC Code 63629-4761-1
Proprietary Name LIDODERM
Package Description 1 PATCH in 1 BOTTLE (63629-4761-1)
Product NDC 63629-4761
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lidocaine
Dosage Form Name PATCH
Route Name CUTANEOUS
Start Marketing Date 19990320
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
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 LIDODERM


General Information