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Lamotrigine - 63739-517-10 - (Lamotrigine)

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Drug Information of Lamotrigine

Product NDC: 63739-517
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: 63739-517
Labeler Name: McKesson Packaging Services a buisness unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090607
Marketing Category: ANDA
Start Marketing Date: 20110608

Package Information of Lamotrigine

Package NDC: 63739-517-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-517-10) > 10 TABLET in 1 BLISTER PACK

NDC Information of Lamotrigine

NDC Code 63739-517-10
Proprietary Name Lamotrigine
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-517-10) > 10 TABLET in 1 BLISTER PACK
Product NDC 63739-517
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lamotrigine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110608
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services a buisness unit of McKesson Corporation
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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