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LAMOTRIGINE - 49349-866-02 - (LAMOTRIGINE)

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Drug Information of LAMOTRIGINE

Product NDC: 49349-866
Proprietary Name: LAMOTRIGINE
Non Proprietary Name: LAMOTRIGINE
Active Ingredient(s): 100    mg/1 & nbsp;   LAMOTRIGINE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of LAMOTRIGINE

Product NDC: 49349-866
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078947
Marketing Category: ANDA
Start Marketing Date: 20130415

Package Information of LAMOTRIGINE

Package NDC: 49349-866-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-866-02)

NDC Information of LAMOTRIGINE

NDC Code 49349-866-02
Proprietary Name LAMOTRIGINE
Package Description 30 TABLET in 1 BLISTER PACK (49349-866-02)
Product NDC 49349-866
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LAMOTRIGINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130415
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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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