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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 050780

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CEFUROXIME AND DEXTROSE IN DUPLEX CONTAINER (CEFUROXIME SODIUM)
EQ 750MG BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: CEFUROXIME SODIUM
Proprietary Name: CEFUROXIME AND DEXTROSE IN DUPLEX CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 750MG BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N050780
Product Number: 001
Approval Date: Feb 21, 2001
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
CEFUROXIME AND DEXTROSE IN DUPLEX CONTAINER (CEFUROXIME SODIUM)
EQ 1.5GM BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: CEFUROXIME SODIUM
Proprietary Name: CEFUROXIME AND DEXTROSE IN DUPLEX CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1.5GM BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N050780
Product Number: 002
Approval Date: Feb 21, 2001
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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