Ribavirin - 0093-7232-81 - (Ribavirin)

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Drug Information of Ribavirin

Product NDC: 0093-7232
Proprietary Name: Ribavirin
Non Proprietary Name: Ribavirin
Active Ingredient(s): 200    mg/1 & nbsp;   Ribavirin
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ribavirin

Product NDC: 0093-7232
Labeler Name: TEVA Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077053
Marketing Category: ANDA
Start Marketing Date: 20051205

Package Information of Ribavirin

Package NDC: 0093-7232-81
Package Description: 168 TABLET, COATED in 1 BOTTLE (0093-7232-81)

NDC Information of Ribavirin

NDC Code 0093-7232-81
Proprietary Name Ribavirin
Package Description 168 TABLET, COATED in 1 BOTTLE (0093-7232-81)
Product NDC 0093-7232
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ribavirin
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20051205
Marketing Category Name ANDA
Labeler Name TEVA Pharmaceuticals USA 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