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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 075763

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NEFAZODONE HYDROCHLORIDE (NEFAZODONE HYDROCHLORIDE)
50MG
Marketing Status: Discontinued
Active Ingredient: NEFAZODONE HYDROCHLORIDE
Proprietary Name: NEFAZODONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A075763
Product Number: 001
Approval Date: Sep 16, 2003
Applicant Holder Full Name: IVAX PHARMACEUTICALS INC SUB TEVA PHARMACEUTICALS USA
Marketing Status:  Discontinued
Patent and Exclusivity Information
NEFAZODONE HYDROCHLORIDE (NEFAZODONE HYDROCHLORIDE)
100MG
Marketing Status: Discontinued
Active Ingredient: NEFAZODONE HYDROCHLORIDE
Proprietary Name: NEFAZODONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A075763
Product Number: 002
Approval Date: Sep 16, 2003
Applicant Holder Full Name: IVAX PHARMACEUTICALS INC SUB TEVA PHARMACEUTICALS USA
Marketing Status:  Discontinued
Patent and Exclusivity Information
NEFAZODONE HYDROCHLORIDE (NEFAZODONE HYDROCHLORIDE)
150MG
Marketing Status: Discontinued
Active Ingredient: NEFAZODONE HYDROCHLORIDE
Proprietary Name: NEFAZODONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 150MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A075763
Product Number: 003
Approval Date: Sep 16, 2003
Applicant Holder Full Name: IVAX PHARMACEUTICALS INC SUB TEVA PHARMACEUTICALS USA
Marketing Status:  Discontinued
Patent and Exclusivity Information
NEFAZODONE HYDROCHLORIDE (NEFAZODONE HYDROCHLORIDE)
200MG
Marketing Status: Discontinued
Active Ingredient: NEFAZODONE HYDROCHLORIDE
Proprietary Name: NEFAZODONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A075763
Product Number: 004
Approval Date: Sep 16, 2003
Applicant Holder Full Name: IVAX PHARMACEUTICALS INC SUB TEVA PHARMACEUTICALS USA
Marketing Status:  Discontinued
Patent and Exclusivity Information
NEFAZODONE HYDROCHLORIDE (NEFAZODONE HYDROCHLORIDE)
250MG
Marketing Status: Discontinued
Active Ingredient: NEFAZODONE HYDROCHLORIDE
Proprietary Name: NEFAZODONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 250MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A075763
Product Number: 005
Approval Date: Sep 16, 2003
Applicant Holder Full Name: IVAX PHARMACEUTICALS INC SUB TEVA PHARMACEUTICALS USA
Marketing Status:  Discontinued
Patent and Exclusivity Information
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