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Lamotrigine - 0143-9964-10 - (Lamotrigine)

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Drug Information of Lamotrigine

Product NDC: 0143-9964
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: 0143-9964
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078134
Marketing Category: ANDA
Start Marketing Date: 20110419

Package Information of Lamotrigine

Package NDC: 0143-9964-10
Package Description: 1000 TABLET in 1 BOTTLE (0143-9964-10)

NDC Information of Lamotrigine

NDC Code 0143-9964-10
Proprietary Name Lamotrigine
Package Description 1000 TABLET in 1 BOTTLE (0143-9964-10)
Product NDC 0143-9964
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lamotrigine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110419
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp
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


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