ribavirin - 54738-953-84 - (ribavirin)

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Drug Information of ribavirin

Product NDC: 54738-953
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: 54738-953
Labeler Name: Richmond Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076203
Marketing Category: ANDA
Start Marketing Date: 20071101

Package Information of ribavirin

Package NDC: 54738-953-84
Package Description: 84 CAPSULE in 1 BOTTLE, PLASTIC (54738-953-84)

NDC Information of ribavirin

NDC Code 54738-953-84
Proprietary Name ribavirin
Package Description 84 CAPSULE in 1 BOTTLE, PLASTIC (54738-953-84)
Product NDC 54738-953
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ribavirin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20071101
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


General Information