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LAMOTRIGINE - 13668-266-28 - (lamotrigine)

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Drug Information of LAMOTRIGINE

Product NDC: 13668-266
Proprietary Name: LAMOTRIGINE
Non Proprietary Name: lamotrigine
Active Ingredient(s):    & nbsp;   lamotrigine
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of LAMOTRIGINE

Product NDC: 13668-266
Labeler Name: Torrent Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078947
Marketing Category: ANDA
Start Marketing Date: 20090914

Package Information of LAMOTRIGINE

Package NDC: 13668-266-28
Package Description: 14 BLISTER PACK in 1 PACKAGE, COMBINATION (13668-266-28) > 1 KIT in 1 BLISTER PACK

NDC Information of LAMOTRIGINE

NDC Code 13668-266-28
Proprietary Name LAMOTRIGINE
Package Description 14 BLISTER PACK in 1 PACKAGE, COMBINATION (13668-266-28) > 1 KIT in 1 BLISTER PACK
Product NDC 13668-266
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lamotrigine
Dosage Form Name KIT
Route Name
Start Marketing Date 20090914
Marketing Category Name ANDA
Labeler Name Torrent Pharmaceuticals Limited
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of LAMOTRIGINE


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