LAMICTAL - 0173-0776-02 - (lamotrigine)

Alphabetical Index


Drug Information of LAMICTAL

Product NDC: 0173-0776
Proprietary Name: LAMICTAL
Non Proprietary Name: lamotrigine
Active Ingredient(s): 100    mg/1 & nbsp;   lamotrigine
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of LAMICTAL

Product NDC: 0173-0776
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022251
Marketing Category: NDA
Start Marketing Date: 20090605

Package Information of LAMICTAL

Package NDC: 0173-0776-02
Package Description: 30 TABLET, ORALLY DISINTEGRATING in 1 DOSE PACK (0173-0776-02)

NDC Information of LAMICTAL

NDC Code 0173-0776-02
Proprietary Name LAMICTAL
Package Description 30 TABLET, ORALLY DISINTEGRATING in 1 DOSE PACK (0173-0776-02)
Product NDC 0173-0776
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lamotrigine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20090605
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name LAMOTRIGINE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]

Complete Information of LAMICTAL


General Information