Product Details for ANDA 077094
RIBAVIRIN (RIBAVIRIN)
200MG
Marketing Status: Prescription
400MG
Marketing Status: Discontinued
500MG
Marketing Status: Discontinued
600MG
Marketing Status: Discontinued
200MG
Marketing Status: Prescription
Active Ingredient: RIBAVIRIN
Proprietary Name: RIBAVIRIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A077094
Product Number: 001
Approval Date: Dec 5, 2005
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status: Prescription
Patent and Exclusivity Information
RIBAVIRIN (RIBAVIRIN)
Proprietary Name: RIBAVIRIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A077094
Product Number: 001
Approval Date: Dec 5, 2005
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status: Prescription
Patent and Exclusivity Information
400MG
Marketing Status: Discontinued
Active Ingredient: RIBAVIRIN
Proprietary Name: RIBAVIRIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 400MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077094
Product Number: 002
Approval Date: Mar 16, 2007
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
RIBAVIRIN (RIBAVIRIN)
Proprietary Name: RIBAVIRIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 400MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077094
Product Number: 002
Approval Date: Mar 16, 2007
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
500MG
Marketing Status: Discontinued
Active Ingredient: RIBAVIRIN
Proprietary Name: RIBAVIRIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077094
Product Number: 004
Approval Date: Apr 18, 2008
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
RIBAVIRIN (RIBAVIRIN)
Proprietary Name: RIBAVIRIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077094
Product Number: 004
Approval Date: Apr 18, 2008
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
600MG
Marketing Status: Discontinued
Active Ingredient: RIBAVIRIN
Proprietary Name: RIBAVIRIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 600MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077094
Product Number: 003
Approval Date: Mar 16, 2007
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: RIBAVIRIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 600MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077094
Product Number: 003
Approval Date: Mar 16, 2007
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information