Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 022217

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VALTURNA (ALISKIREN HEMIFUMARATE; VALSARTAN)
EQ 150MG BASE;160MG Marketing Status: Discontinued

Active Ingredient: ALISKIREN HEMIFUMARATE; VALSARTAN
Proprietary Name: VALTURNA
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 150MG BASE;160MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N022217
Product Number: 001
Approval Date: Sep 16, 2009
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information

VALTURNA (ALISKIREN HEMIFUMARATE; VALSARTAN)
EQ 300MG BASE;320MG Marketing Status: Discontinued

Active Ingredient: ALISKIREN HEMIFUMARATE; VALSARTAN
Proprietary Name: VALTURNA
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 300MG BASE;320MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N022217
Product Number: 002
Approval Date: Sep 16, 2009
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information

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