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Lamotrigine - 51672-4132-3 - (Lamotrigine)

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Drug Information of Lamotrigine

Product NDC: 51672-4132
Proprietary Name: Lamotrigine
Non Proprietary Name: Lamotrigine
Active Ingredient(s): 150    mg/1 & nbsp;   Lamotrigine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lamotrigine

Product NDC: 51672-4132
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: 51672-4132-3
Package Description: 1000 TABLET in 1 BOTTLE (51672-4132-3)

NDC Information of Lamotrigine

NDC Code 51672-4132-3
Proprietary Name Lamotrigine
Package Description 1000 TABLET in 1 BOTTLE (51672-4132-3)
Product NDC 51672-4132
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 150
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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