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Lamotrigine - 64679-271-02 - (Lamotrigine)

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Drug Information of Lamotrigine

Product NDC: 64679-271
Proprietary Name: Lamotrigine
Non Proprietary Name: Lamotrigine
Active Ingredient(s): 25    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: 64679-271
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202498
Marketing Category: ANDA
Start Marketing Date: 20121129

Package Information of Lamotrigine

Package NDC: 64679-271-02
Package Description: 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (64679-271-02)

NDC Information of Lamotrigine

NDC Code 64679-271-02
Proprietary Name Lamotrigine
Package Description 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (64679-271-02)
Product NDC 64679-271
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lamotrigine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20121129
Marketing Category Name ANDA
Labeler Name Wockhardt USA LLC.
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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