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Lamotrigine - 65841-682-10 - (Lamotrigine)

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Drug Information of Lamotrigine

Product NDC: 65841-682
Proprietary Name: Lamotrigine
Non Proprietary Name: Lamotrigine
Active Ingredient(s): 25    mg/1 & nbsp;   Lamotrigine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lamotrigine

Product NDC: 65841-682
Labeler Name: Cadila Healthcare Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077633
Marketing Category: ANDA
Start Marketing Date: 20090127

Package Information of Lamotrigine

Package NDC: 65841-682-10
Package Description: 1000 TABLET in 1 BOTTLE (65841-682-10)

NDC Information of Lamotrigine

NDC Code 65841-682-10
Proprietary Name Lamotrigine
Package Description 1000 TABLET in 1 BOTTLE (65841-682-10)
Product NDC 65841-682
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 Cadila Healthcare 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


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