Ribasphere - 66435-101-56 - (Ribavirin)

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Drug Information of Ribasphere

Product NDC: 66435-101
Proprietary Name: Ribasphere
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 Ribasphere

Product NDC: 66435-101
Labeler Name: Kadmon Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076203
Marketing Category: ANDA
Start Marketing Date: 20040407

Package Information of Ribasphere

Package NDC: 66435-101-56
Package Description: 56 CAPSULE in 1 BOTTLE, PLASTIC (66435-101-56)

NDC Information of Ribasphere

NDC Code 66435-101-56
Proprietary Name Ribasphere
Package Description 56 CAPSULE in 1 BOTTLE, PLASTIC (66435-101-56)
Product NDC 66435-101
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ribavirin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20040407
Marketing Category Name ANDA
Labeler Name Kadmon Pharmaceuticals, LLC
Substance Name RIBAVIRIN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antiviral [EPC]

Complete Information of Ribasphere


General Information