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Lamotrigine - 16714-374-04 - (Lamotrigine)

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Drug Information of Lamotrigine

Product NDC: 16714-374
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: 16714-374
Labeler Name: NorthStar RxLLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090607
Marketing Category: ANDA
Start Marketing Date: 20110125

Package Information of Lamotrigine

Package NDC: 16714-374-04
Package Description: 60 TABLET in 1 BOTTLE (16714-374-04)

NDC Information of Lamotrigine

NDC Code 16714-374-04
Proprietary Name Lamotrigine
Package Description 60 TABLET in 1 BOTTLE (16714-374-04)
Product NDC 16714-374
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lamotrigine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110125
Marketing Category Name ANDA
Labeler Name NorthStar RxLLC
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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