Ribavirin - 68382-127-17 - (Ribavirin)

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Drug Information of Ribavirin

Product NDC: 68382-127
Proprietary Name: Ribavirin
Non Proprietary Name: Ribavirin
Active Ingredient(s): 400    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: 68382-127
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077094
Marketing Category: ANDA
Start Marketing Date: 20051205

Package Information of Ribavirin

Package NDC: 68382-127-17
Package Description: 28 TABLET, FILM COATED in 1 BOTTLE (68382-127-17)

NDC Information of Ribavirin

NDC Code 68382-127-17
Proprietary Name Ribavirin
Package Description 28 TABLET, FILM COATED in 1 BOTTLE (68382-127-17)
Product NDC 68382-127
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 Zydus Pharmaceuticals (USA) Inc.
Substance Name RIBAVIRIN
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antiviral [EPC]

Complete Information of Ribavirin


General Information