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Lamotrigine - 68382-109-01 - (Lamotrigine)

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Drug Information of Lamotrigine

Product NDC: 68382-109
Proprietary Name: Lamotrigine
Non Proprietary Name: Lamotrigine
Active Ingredient(s): 25    mg/1 & nbsp;   Lamotrigine
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Lamotrigine

Product NDC: 68382-109
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078009
Marketing Category: ANDA
Start Marketing Date: 20090123

Package Information of Lamotrigine

Package NDC: 68382-109-01
Package Description: 100 TABLET, CHEWABLE in 1 BOTTLE (68382-109-01)

NDC Information of Lamotrigine

NDC Code 68382-109-01
Proprietary Name Lamotrigine
Package Description 100 TABLET, CHEWABLE in 1 BOTTLE (68382-109-01)
Product NDC 68382-109
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lamotrigine
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20090123
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) 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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