ribavirin - 54738-950-16 - (ribavirin)

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Drug Information of ribavirin

Product NDC: 54738-950
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: 54738-950
Labeler Name: Richmond Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077456
Marketing Category: ANDA
Start Marketing Date: 20080601

Package Information of ribavirin

Package NDC: 54738-950-16
Package Description: 168 TABLET, FILM COATED in 1 BOTTLE (54738-950-16)

NDC Information of ribavirin

NDC Code 54738-950-16
Proprietary Name ribavirin
Package Description 168 TABLET, FILM COATED in 1 BOTTLE (54738-950-16)
Product NDC 54738-950
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ribavirin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080601
Marketing Category Name ANDA
Labeler Name Richmond Pharmaceuticals, 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


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