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Lamotrigine - 55111-719-05 - (Lamotrigine)

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Drug Information of Lamotrigine

Product NDC: 55111-719
Proprietary Name: Lamotrigine
Non Proprietary Name: Lamotrigine
Active Ingredient(s): 100    mg/1 & nbsp;   Lamotrigine
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Lamotrigine

Product NDC: 55111-719
Labeler Name: Dr.Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202383
Marketing Category: ANDA
Start Marketing Date: 20130620

Package Information of Lamotrigine

Package NDC: 55111-719-05
Package Description: 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-719-05)

NDC Information of Lamotrigine

NDC Code 55111-719-05
Proprietary Name Lamotrigine
Package Description 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-719-05)
Product NDC 55111-719
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lamotrigine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130620
Marketing Category Name ANDA
Labeler Name Dr.Reddy's Laboratories Limited
Substance Name LAMOTRIGINE
Strength Number 100
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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