LIDODERM - 49999-419-30 - (LIDODERM)

Alphabetical Index


Drug Information of LIDODERM

Product NDC: 49999-419
Proprietary Name: LIDODERM
Non Proprietary Name: LIDODERM
Active Ingredient(s): 700    mg/1 & nbsp;   LIDODERM
Administration Route(s): CUTANEOUS
Dosage Form(s): PATCH
Coding System: National Drug Codes(NDC)

Labeler Information of LIDODERM

Product NDC: 49999-419
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020612
Marketing Category: NDA
Start Marketing Date: 20111201

Package Information of LIDODERM

Package NDC: 49999-419-30
Package Description: 30 POUCH in 1 CARTON (49999-419-30) > 1 PATCH in 1 POUCH

NDC Information of LIDODERM

NDC Code 49999-419-30
Proprietary Name LIDODERM
Package Description 30 POUCH in 1 CARTON (49999-419-30) > 1 PATCH in 1 POUCH
Product NDC 49999-419
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LIDODERM
Dosage Form Name PATCH
Route Name CUTANEOUS
Start Marketing Date 20111201
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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