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LAMOTRIGINE - 43063-202-90 - (LAMOTRIGINE)

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Drug Information of LAMOTRIGINE

Product NDC: 43063-202
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: 43063-202
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078947
Marketing Category: ANDA
Start Marketing Date: 20090127

Package Information of LAMOTRIGINE

Package NDC: 43063-202-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (43063-202-90)

NDC Information of LAMOTRIGINE

NDC Code 43063-202-90
Proprietary Name LAMOTRIGINE
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (43063-202-90)
Product NDC 43063-202
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LAMOTRIGINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090127
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
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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