Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 050551

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CEFOBID (CEFOPERAZONE SODIUM)
EQ 1GM BASE/VIAL
Marketing Status: Discontinued

Active Ingredient: CEFOPERAZONE SODIUM
Proprietary Name: CEFOBID
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N050551
Product Number: 001
Approval Date: Nov 18, 1982
Applicant Holder Full Name: PFIZER LABORATORIES DIV PFIZER INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

CEFOBID (CEFOPERAZONE SODIUM)
EQ 2GM BASE/VIAL
Marketing Status: Discontinued

Active Ingredient: CEFOPERAZONE SODIUM
Proprietary Name: CEFOBID
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 2GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N050551
Product Number: 002
Approval Date: Nov 18, 1982
Applicant Holder Full Name: PFIZER LABORATORIES DIV PFIZER INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

CEFOBID (CEFOPERAZONE SODIUM)
EQ 10GM BASE/VIAL
Marketing Status: Discontinued

Active Ingredient: CEFOPERAZONE SODIUM
Proprietary Name: CEFOBID
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 10GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N050551
Product Number: 003
Approval Date: Mar 5, 1990
Applicant Holder Full Name: PFIZER LABORATORIES DIV PFIZER INC
Marketing Status:  Discontinued
Patent and Exclusivity Information