Modafinil - 59115-069-01 - (modafinil)

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Drug Information of Modafinil

Product NDC: 59115-069
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: 59115-069
Labeler Name: Hikma Pharmaceutical
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090543
Marketing Category: ANDA
Start Marketing Date: 20080404

Package Information of Modafinil

Package NDC: 59115-069-01
Package Description: 100 TABLET in 1 BOTTLE (59115-069-01)

NDC Information of Modafinil

NDC Code 59115-069-01
Proprietary Name Modafinil
Package Description 100 TABLET in 1 BOTTLE (59115-069-01)
Product NDC 59115-069
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name modafinil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080404
Marketing Category Name ANDA
Labeler Name Hikma Pharmaceutical
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