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Lamotrigine - 54868-5955-1 - (Lamotrigine)

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Drug Information of Lamotrigine

Product NDC: 54868-5955
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: 54868-5955
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076388
Marketing Category: ANDA
Start Marketing Date: 20081205

Package Information of Lamotrigine

Package NDC: 54868-5955-1
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (54868-5955-1)

NDC Information of Lamotrigine

NDC Code 54868-5955-1
Proprietary Name Lamotrigine
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (54868-5955-1)
Product NDC 54868-5955
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lamotrigine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081205
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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


General Information