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Lamotrigine Extended Release - 49884-564-01 - (lamotrigine extended release)

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Drug Information of Lamotrigine Extended Release

Product NDC: 49884-564
Proprietary Name: Lamotrigine Extended Release
Non Proprietary Name: lamotrigine extended release
Active Ingredient(s): 200    mg/1 & nbsp;   lamotrigine extended release
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lamotrigine Extended Release

Product NDC: 49884-564
Labeler Name: Par Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201791
Marketing Category: ANDA
Start Marketing Date: 20130118

Package Information of Lamotrigine Extended Release

Package NDC: 49884-564-01
Package Description: 100 TABLET in 1 BOTTLE (49884-564-01)

NDC Information of Lamotrigine Extended Release

NDC Code 49884-564-01
Proprietary Name Lamotrigine Extended Release
Package Description 100 TABLET in 1 BOTTLE (49884-564-01)
Product NDC 49884-564
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lamotrigine extended release
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130118
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical Inc.
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 Extended Release


General Information