LAMICTAL - 55289-410-30 - (lamotrigine)

Alphabetical Index


Drug Information of LAMICTAL

Product NDC: 55289-410
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: 55289-410
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020241
Marketing Category: NDA
Start Marketing Date: 19950117

Package Information of LAMICTAL

Package NDC: 55289-410-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (55289-410-30)

NDC Information of LAMICTAL

NDC Code 55289-410-30
Proprietary Name LAMICTAL
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (55289-410-30)
Product NDC 55289-410
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lamotrigine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19950117
Marketing Category Name NDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
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