LAMICTAL - 21695-223-30 - (lamotrigine)

Alphabetical Index


Drug Information of LAMICTAL

Product NDC: 21695-223
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: 21695-223
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020241
Marketing Category: NDA
Start Marketing Date: 19950117

Package Information of LAMICTAL

Package NDC: 21695-223-30
Package Description: 30 TABLET in 1 BOTTLE (21695-223-30)

NDC Information of LAMICTAL

NDC Code 21695-223-30
Proprietary Name LAMICTAL
Package Description 30 TABLET in 1 BOTTLE (21695-223-30)
Product NDC 21695-223
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 Rebel Distributors Corp
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