LIDODERM - 21695-075-01 - (Lidocaine)

Alphabetical Index


Drug Information of LIDODERM

Product NDC: 21695-075
Proprietary Name: LIDODERM
Non Proprietary Name: Lidocaine
Active Ingredient(s): 700    mg/12h & nbsp;   Lidocaine
Administration Route(s): CUTANEOUS
Dosage Form(s): PATCH
Coding System: National Drug Codes(NDC)

Labeler Information of LIDODERM

Product NDC: 21695-075
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020612
Marketing Category: NDA
Start Marketing Date: 20100201

Package Information of LIDODERM

Package NDC: 21695-075-01
Package Description: 1 PATCH in 1 POUCH (21695-075-01) > 12 h in 1 PATCH

NDC Information of LIDODERM

NDC Code 21695-075-01
Proprietary Name LIDODERM
Package Description 1 PATCH in 1 POUCH (21695-075-01) > 12 h in 1 PATCH
Product NDC 21695-075
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine
Dosage Form Name PATCH
Route Name CUTANEOUS
Start Marketing Date 20100201
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp.
Substance Name LIDOCAINE
Strength Number 700
Strength Unit mg/12h
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE]

Complete Information of LIDODERM


General Information