LAMICTAL - 0173-0594-02 - (lamotrigine)

Alphabetical Index


Drug Information of LAMICTAL

Product NDC: 0173-0594
Proprietary Name: LAMICTAL
Non Proprietary Name: lamotrigine
Active Ingredient(s):    & nbsp;   lamotrigine
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of LAMICTAL

Product NDC: 0173-0594
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020241
Marketing Category: NDA
Start Marketing Date: 20030929

Package Information of LAMICTAL

Package NDC: 0173-0594-02
Package Description: 1 BLISTER PACK in 1 PACKAGE, COMBINATION (0173-0594-02) > 1 KIT in 1 BLISTER PACK

NDC Information of LAMICTAL

NDC Code 0173-0594-02
Proprietary Name LAMICTAL
Package Description 1 BLISTER PACK in 1 PACKAGE, COMBINATION (0173-0594-02) > 1 KIT in 1 BLISTER PACK
Product NDC 0173-0594
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lamotrigine
Dosage Form Name KIT
Route Name
Start Marketing Date 20030929
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of LAMICTAL


General Information