Ribavirin - 0781-2043-10 - (Ribavirin)

Alphabetical Index


Drug Information of Ribavirin

Product NDC: 0781-2043
Proprietary Name: Ribavirin
Non Proprietary Name: Ribavirin
Active Ingredient(s): 200    mg/1 & nbsp;   Ribavirin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Ribavirin

Product NDC: 0781-2043
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076192
Marketing Category: ANDA
Start Marketing Date: 20040406

Package Information of Ribavirin

Package NDC: 0781-2043-10
Package Description: 1000 CAPSULE in 1 BOTTLE (0781-2043-10)

NDC Information of Ribavirin

NDC Code 0781-2043-10
Proprietary Name Ribavirin
Package Description 1000 CAPSULE in 1 BOTTLE (0781-2043-10)
Product NDC 0781-2043
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ribavirin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20040406
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