Modafinil - 65862-602-05 - (Modafinil)

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Drug Information of Modafinil

Product NDC: 65862-602
Proprietary Name: Modafinil
Non Proprietary Name: Modafinil
Active Ingredient(s): 200    mg/1 & nbsp;   Modafinil
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Modafinil

Product NDC: 65862-602
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202566
Marketing Category: ANDA
Start Marketing Date: 20120927

Package Information of Modafinil

Package NDC: 65862-602-05
Package Description: 500 TABLET in 1 BOTTLE (65862-602-05)

NDC Information of Modafinil

NDC Code 65862-602-05
Proprietary Name Modafinil
Package Description 500 TABLET in 1 BOTTLE (65862-602-05)
Product NDC 65862-602
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Modafinil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120927
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name MODAFINIL
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Central Nervous System Stimulation [PE],Increased Sympathetic Activity [PE],Sympathomimetic-like Agent [EPC]

Complete Information of Modafinil


General Information