LAMICTAL - 0173-0527-00 - (lamotrigine)

Alphabetical Index


Drug Information of LAMICTAL

Product NDC: 0173-0527
Proprietary Name: LAMICTAL
Non Proprietary Name: lamotrigine
Active Ingredient(s): 25    mg/1 & nbsp;   lamotrigine
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of LAMICTAL

Product NDC: 0173-0527
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020764
Marketing Category: NDA
Start Marketing Date: 19980903

Package Information of LAMICTAL

Package NDC: 0173-0527-00
Package Description: 100 TABLET, CHEWABLE in 1 BOTTLE (0173-0527-00)

NDC Information of LAMICTAL

NDC Code 0173-0527-00
Proprietary Name LAMICTAL
Package Description 100 TABLET, CHEWABLE in 1 BOTTLE (0173-0527-00)
Product NDC 0173-0527
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lamotrigine
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 19980903
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name LAMOTRIGINE
Strength Number 25
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