LAMICTAL - 0173-0644-60 - (lamotrigine)

Alphabetical Index


Drug Information of LAMICTAL

Product NDC: 0173-0644
Proprietary Name: LAMICTAL
Non Proprietary Name: lamotrigine
Active Ingredient(s): 200    mg/1 & nbsp;   lamotrigine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of LAMICTAL

Product NDC: 0173-0644
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020241
Marketing Category: NDA
Start Marketing Date: 19950118

Package Information of LAMICTAL

Package NDC: 0173-0644-60
Package Description: 60 TABLET in 1 BOTTLE (0173-0644-60)

NDC Information of LAMICTAL

NDC Code 0173-0644-60
Proprietary Name LAMICTAL
Package Description 60 TABLET in 1 BOTTLE (0173-0644-60)
Product NDC 0173-0644
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lamotrigine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19950118
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name LAMOTRIGINE
Strength Number 200
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