Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 050684

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ZOSYN (PIPERACILLIN SODIUM; TAZOBACTAM SODIUM)
EQ 2GM BASE/VIAL;EQ 250MG BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: PIPERACILLIN SODIUM; TAZOBACTAM SODIUM
Proprietary Name: ZOSYN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 2GM BASE/VIAL;EQ 250MG BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N050684
Product Number: 001
Approval Date: Oct 22, 1993
Applicant Holder Full Name: WYETH PHARMACEUTICALS LLC
Marketing Status:  Discontinued
Patent and Exclusivity Information
ZOSYN (PIPERACILLIN SODIUM; TAZOBACTAM SODIUM)
EQ 3GM BASE/VIAL;EQ 375MG BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: PIPERACILLIN SODIUM; TAZOBACTAM SODIUM
Proprietary Name: ZOSYN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 3GM BASE/VIAL;EQ 375MG BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N050684
Product Number: 002
Approval Date: Oct 22, 1993
Applicant Holder Full Name: WYETH PHARMACEUTICALS LLC
Marketing Status:  Discontinued
Patent and Exclusivity Information
ZOSYN (PIPERACILLIN SODIUM; TAZOBACTAM SODIUM)
EQ 4GM BASE/VIAL;EQ 500MG BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: PIPERACILLIN SODIUM; TAZOBACTAM SODIUM
Proprietary Name: ZOSYN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 4GM BASE/VIAL;EQ 500MG BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N050684
Product Number: 003
Approval Date: Oct 22, 1993
Applicant Holder Full Name: WYETH PHARMACEUTICALS LLC
Marketing Status:  Discontinued
Patent and Exclusivity Information
ZOSYN (PIPERACILLIN SODIUM; TAZOBACTAM SODIUM)
EQ 36GM BASE/VIAL;EQ 4.5GM BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: PIPERACILLIN SODIUM; TAZOBACTAM SODIUM
Proprietary Name: ZOSYN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 36GM BASE/VIAL;EQ 4.5GM BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N050684
Product Number: 004
Approval Date: Oct 22, 1993
Applicant Holder Full Name: WYETH PHARMACEUTICALS LLC
Marketing Status:  Discontinued
Patent and Exclusivity Information

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