Riluzole - 62756-538-18 - (Riluzole)

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Drug Information of Riluzole

Product NDC: 62756-538
Proprietary Name: Riluzole
Non Proprietary Name: Riluzole
Active Ingredient(s): 50    mg/1 & nbsp;   Riluzole
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Riluzole

Product NDC: 62756-538
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091417
Marketing Category: ANDA
Start Marketing Date: 20130618

Package Information of Riluzole

Package NDC: 62756-538-18
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (62756-538-18)

NDC Information of Riluzole

NDC Code 62756-538-18
Proprietary Name Riluzole
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (62756-538-18)
Product NDC 62756-538
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Riluzole
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130618
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
Substance Name RILUZOLE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Benzothiazole [EPC],Benzothiazoles [Chemical/Ingredient]

Complete Information of Riluzole


General Information