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lamotrigine - 0245-0223-15 - (Lamotrigine)

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Drug Information of lamotrigine

Product NDC: 0245-0223
Proprietary Name: lamotrigine
Non Proprietary Name: Lamotrigine
Active Ingredient(s): 150    mg/1 & nbsp;   Lamotrigine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of lamotrigine

Product NDC: 0245-0223
Labeler Name: Upsher-Smith Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078310
Marketing Category: ANDA
Start Marketing Date: 20110228

Package Information of lamotrigine

Package NDC: 0245-0223-15
Package Description: 500 TABLET in 1 BOTTLE (0245-0223-15)

NDC Information of lamotrigine

NDC Code 0245-0223-15
Proprietary Name lamotrigine
Package Description 500 TABLET in 1 BOTTLE (0245-0223-15)
Product NDC 0245-0223
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lamotrigine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110228
Marketing Category Name ANDA
Labeler Name Upsher-Smith Laboratories, Inc.
Substance Name LAMOTRIGINE
Strength Number 150
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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