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Lamotrigine - 0781-5122-10 - (Lamotrigine)

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Drug Information of Lamotrigine

Product NDC: 0781-5122
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: 0781-5122
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078645
Marketing Category: ANDA
Start Marketing Date: 20100105

Package Information of Lamotrigine

Package NDC: 0781-5122-10
Package Description: 1000 TABLET in 1 BOTTLE (0781-5122-10)

NDC Information of Lamotrigine

NDC Code 0781-5122-10
Proprietary Name Lamotrigine
Package Description 1000 TABLET in 1 BOTTLE (0781-5122-10)
Product NDC 0781-5122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lamotrigine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100105
Marketing Category Name ANDA
Labeler Name Sandoz Inc
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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