Modafinil - 60505-2526-1 - (modafinil)

Alphabetical Index


Drug Information of Modafinil

Product NDC: 60505-2526
Proprietary Name: Modafinil
Non Proprietary Name: modafinil
Active Ingredient(s): 100    mg/1 & nbsp;   modafinil
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Modafinil

Product NDC: 60505-2526
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077667
Marketing Category: ANDA
Start Marketing Date: 20120926

Package Information of Modafinil

Package NDC: 60505-2526-1
Package Description: 100 TABLET in 1 BOTTLE (60505-2526-1)

NDC Information of Modafinil

NDC Code 60505-2526-1
Proprietary Name Modafinil
Package Description 100 TABLET in 1 BOTTLE (60505-2526-1)
Product NDC 60505-2526
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name modafinil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120926
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name MODAFINIL
Strength Number 100
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