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Lamotrigine - 55111-220-05 - (Lamotrigine)

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Drug Information of Lamotrigine

Product NDC: 55111-220
Proprietary Name: Lamotrigine
Non Proprietary Name: Lamotrigine
Active Ingredient(s): 25    mg/1 & nbsp;   Lamotrigine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lamotrigine

Product NDC: 55111-220
Labeler Name: Dr.Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076708
Marketing Category: ANDA
Start Marketing Date: 20090129

Package Information of Lamotrigine

Package NDC: 55111-220-05
Package Description: 500 TABLET in 1 BOTTLE (55111-220-05)

NDC Information of Lamotrigine

NDC Code 55111-220-05
Proprietary Name Lamotrigine
Package Description 500 TABLET in 1 BOTTLE (55111-220-05)
Product NDC 55111-220
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lamotrigine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090129
Marketing Category Name ANDA
Labeler Name Dr.Reddy's Laboratories Limited
Substance Name LAMOTRIGINE
Strength Number 25
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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