PROVIGIL - 21695-235-30 - (MODAFINIL)

Alphabetical Index


Drug Information of PROVIGIL

Product NDC: 21695-235
Proprietary Name: PROVIGIL
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 PROVIGIL

Product NDC: 21695-235
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020717
Marketing Category: NDA
Start Marketing Date: 20040119

Package Information of PROVIGIL

Package NDC: 21695-235-30
Package Description: 30 TABLET in 1 BOTTLE (21695-235-30)

NDC Information of PROVIGIL

NDC Code 21695-235-30
Proprietary Name PROVIGIL
Package Description 30 TABLET in 1 BOTTLE (21695-235-30)
Product NDC 21695-235
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MODAFINIL
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040119
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
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 PROVIGIL


General Information