Ribavirin - 0781-5177-04 - (Ribavirin)

Alphabetical Index


Drug Information of Ribavirin

Product NDC: 0781-5177
Proprietary Name: Ribavirin
Non Proprietary Name: Ribavirin
Active Ingredient(s): 200    mg/1 & nbsp;   Ribavirin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ribavirin

Product NDC: 0781-5177
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077743
Marketing Category: ANDA
Start Marketing Date: 20061003

Package Information of Ribavirin

Package NDC: 0781-5177-04
Package Description: 84 TABLET, FILM COATED in 1 BOTTLE (0781-5177-04)

NDC Information of Ribavirin

NDC Code 0781-5177-04
Proprietary Name Ribavirin
Package Description 84 TABLET, FILM COATED in 1 BOTTLE (0781-5177-04)
Product NDC 0781-5177
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ribavirin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20061003
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name RIBAVIRIN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antiviral [EPC]

Complete Information of Ribavirin


General Information