LAMICTAL - 54868-4673-0 - (lamotrigine)

Alphabetical Index


Drug Information of LAMICTAL

Product NDC: 54868-4673
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: 54868-4673
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020241
Marketing Category: NDA
Start Marketing Date: 20110216

Package Information of LAMICTAL

Package NDC: 54868-4673-0
Package Description: 10 TABLET in 1 BOTTLE, PLASTIC (54868-4673-0)

NDC Information of LAMICTAL

NDC Code 54868-4673-0
Proprietary Name LAMICTAL
Package Description 10 TABLET in 1 BOTTLE, PLASTIC (54868-4673-0)
Product NDC 54868-4673
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lamotrigine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110216
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
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