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Lamotrigine - 76237-262-30 - (Lamotrigine)

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Drug Information of Lamotrigine

Product NDC: 76237-262
Proprietary Name: Lamotrigine
Non Proprietary Name: Lamotrigine
Active Ingredient(s): 25    mg/1 & nbsp;   Lamotrigine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lamotrigine

Product NDC: 76237-262
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076388
Marketing Category: ANDA
Start Marketing Date: 20111130

Package Information of Lamotrigine

Package NDC: 76237-262-30
Package Description: 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-262-30) > 5 TABLET in 1 BLISTER PACK

NDC Information of Lamotrigine

NDC Code 76237-262-30
Proprietary Name Lamotrigine
Package Description 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-262-30) > 5 TABLET in 1 BLISTER PACK
Product NDC 76237-262
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lamotrigine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111130
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
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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