LAMICTAL - 35356-162-00 - (lamotrigine)

Alphabetical Index


Drug Information of LAMICTAL

Product NDC: 35356-162
Proprietary Name: LAMICTAL
Non Proprietary Name: lamotrigine
Active Ingredient(s): 100    mg/1 & nbsp;   lamotrigine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of LAMICTAL

Product NDC: 35356-162
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020241
Marketing Category: NDA
Start Marketing Date: 20120229

Package Information of LAMICTAL

Package NDC: 35356-162-00
Package Description: 100 TABLET in 1 BOTTLE (35356-162-00)

NDC Information of LAMICTAL

NDC Code 35356-162-00
Proprietary Name LAMICTAL
Package Description 100 TABLET in 1 BOTTLE (35356-162-00)
Product NDC 35356-162
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lamotrigine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120229
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products 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