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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 206181

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VORICONAZOLE (VORICONAZOLE)
50MG
Marketing Status: Prescription
Active Ingredient: VORICONAZOLE
Proprietary Name: VORICONAZOLE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A206181
Product Number: 001
Approval Date: May 24, 2016
Applicant Holder Full Name: AJANTA PHARMA LTD
Marketing Status:  Prescription
Patent and Exclusivity Information
VORICONAZOLE (VORICONAZOLE)
200MG
Marketing Status: Prescription
Active Ingredient: VORICONAZOLE
Proprietary Name: VORICONAZOLE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A206181
Product Number: 002
Approval Date: May 24, 2016
Applicant Holder Full Name: AJANTA PHARMA LTD
Marketing Status:  Prescription
Patent and Exclusivity Information
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