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Lamotrigine - 51672-4133-1 - (Lamotrigine)

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Drug Information of Lamotrigine

Product NDC: 51672-4133
Proprietary Name: Lamotrigine
Non Proprietary Name: Lamotrigine
Active Ingredient(s): 200    mg/1 & nbsp;   Lamotrigine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lamotrigine

Product NDC: 51672-4133
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078525
Marketing Category: ANDA
Start Marketing Date: 20090127

Package Information of Lamotrigine

Package NDC: 51672-4133-1
Package Description: 100 TABLET in 1 BOTTLE (51672-4133-1)

NDC Information of Lamotrigine

NDC Code 51672-4133-1
Proprietary Name Lamotrigine
Package Description 100 TABLET in 1 BOTTLE (51672-4133-1)
Product NDC 51672-4133
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lamotrigine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090127
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name LAMOTRIGINE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]

Complete Information of Lamotrigine


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