Ribavirin - 65841-046-30 - (Ribavirin)

Alphabetical Index


Drug Information of Ribavirin

Product NDC: 65841-046
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: 65841-046
Labeler Name: Cadila Healthcare Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077094
Marketing Category: ANDA
Start Marketing Date: 20051205

Package Information of Ribavirin

Package NDC: 65841-046-30
Package Description: 10 BLISTER PACK in 1 CARTON (65841-046-30) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Ribavirin

NDC Code 65841-046-30
Proprietary Name Ribavirin
Package Description 10 BLISTER PACK in 1 CARTON (65841-046-30) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 65841-046
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ribavirin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20051205
Marketing Category Name ANDA
Labeler Name Cadila Healthcare Limited
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