LAMICTAL - 0173-0633-10 - (lamotrigine)

Alphabetical Index


Drug Information of LAMICTAL

Product NDC: 0173-0633
Proprietary Name: LAMICTAL
Non Proprietary Name: lamotrigine
Active Ingredient(s): 25    mg/1 & nbsp;   lamotrigine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of LAMICTAL

Product NDC: 0173-0633
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020241
Marketing Category: NDA
Start Marketing Date: 19960815

Package Information of LAMICTAL

Package NDC: 0173-0633-10
Package Description: 35 TABLET in 1 DOSE PACK (0173-0633-10)

NDC Information of LAMICTAL

NDC Code 0173-0633-10
Proprietary Name LAMICTAL
Package Description 35 TABLET in 1 DOSE PACK (0173-0633-10)
Product NDC 0173-0633
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lamotrigine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19960815
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