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Lamotrigine - 65862-362-81 - (Lamotrigine)

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Drug Information of Lamotrigine

Product NDC: 65862-362
Proprietary Name: Lamotrigine
Non Proprietary Name: Lamotrigine
Active Ingredient(s): 25    mg/1 & nbsp;   Lamotrigine
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Lamotrigine

Product NDC: 65862-362
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090401
Marketing Category: ANDA
Start Marketing Date: 20091104

Package Information of Lamotrigine

Package NDC: 65862-362-81
Package Description: 8000 TABLET, CHEWABLE in 1 BOTTLE (65862-362-81)

NDC Information of Lamotrigine

NDC Code 65862-362-81
Proprietary Name Lamotrigine
Package Description 8000 TABLET, CHEWABLE in 1 BOTTLE (65862-362-81)
Product NDC 65862-362
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lamotrigine
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20091104
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name LAMOTRIGINE
Strength Number 25
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


General Information