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Lamotrigine - 0615-7545-39 - (Lamotrigine)

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Drug Information of Lamotrigine

Product NDC: 0615-7545
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: 0615-7545
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076388
Marketing Category: ANDA
Start Marketing Date: 20100427

Package Information of Lamotrigine

Package NDC: 0615-7545-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-7545-39)

NDC Information of Lamotrigine

NDC Code 0615-7545-39
Proprietary Name Lamotrigine
Package Description 30 TABLET in 1 BLISTER PACK (0615-7545-39)
Product NDC 0615-7545
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lamotrigine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100427
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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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