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Lamotrigine - 59115-066-01 - (Lamotrigine)

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Drug Information of Lamotrigine

Product NDC: 59115-066
Proprietary Name: Lamotrigine
Non Proprietary Name: Lamotrigine
Active Ingredient(s): 100    mg/1 & nbsp;   Lamotrigine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lamotrigine

Product NDC: 59115-066
Labeler Name: Hikma Pharmaceutical
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078134
Marketing Category: ANDA
Start Marketing Date: 20110419

Package Information of Lamotrigine

Package NDC: 59115-066-01
Package Description: 100 TABLET in 1 BOTTLE (59115-066-01)

NDC Information of Lamotrigine

NDC Code 59115-066-01
Proprietary Name Lamotrigine
Package Description 100 TABLET in 1 BOTTLE (59115-066-01)
Product NDC 59115-066
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lamotrigine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110419
Marketing Category Name ANDA
Labeler Name Hikma Pharmaceutical
Substance Name LAMOTRIGINE
Strength Number 100
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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