Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 075572

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BUSPIRONE HYDROCHLORIDE (BUSPIRONE HYDROCHLORIDE)
5MG
Marketing Status: Discontinued

Active Ingredient: BUSPIRONE HYDROCHLORIDE
Proprietary Name: BUSPIRONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A075572
Product Number: 001
Approval Date: Feb 27, 2002
Applicant Holder Full Name: NESHER PHARMACEUTICALS USA LLC
Marketing Status:  Discontinued
Patent and Exclusivity Information

BUSPIRONE HYDROCHLORIDE (BUSPIRONE HYDROCHLORIDE)
10MG
Marketing Status: Discontinued

Active Ingredient: BUSPIRONE HYDROCHLORIDE
Proprietary Name: BUSPIRONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A075572
Product Number: 002
Approval Date: Feb 27, 2002
Applicant Holder Full Name: NESHER PHARMACEUTICALS USA LLC
Marketing Status:  Discontinued
Patent and Exclusivity Information

BUSPIRONE HYDROCHLORIDE (BUSPIRONE HYDROCHLORIDE)
15MG
Marketing Status: Discontinued

Active Ingredient: BUSPIRONE HYDROCHLORIDE
Proprietary Name: BUSPIRONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 15MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A075572
Product Number: 003
Approval Date: Feb 27, 2002
Applicant Holder Full Name: NESHER PHARMACEUTICALS USA LLC
Marketing Status:  Discontinued
Patent and Exclusivity Information