Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 050792

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CEFOTAXIME AND DEXTROSE 2.4% IN PLASTIC CONTAINER (CEFOTAXIME SODIUM)
EQ 2GM BASE
Marketing Status: Discontinued

Active Ingredient: CEFOTAXIME SODIUM
Proprietary Name: CEFOTAXIME AND DEXTROSE 2.4% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 2GM BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N050792
Product Number: 001
Approval Date: Jul 29, 2004
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

CEFOTAXIME AND DEXTROSE 3.9% IN PLASTIC CONTAINER (CEFOTAXIME SODIUM)
EQ 1GM BASE
Marketing Status: Discontinued

Active Ingredient: CEFOTAXIME SODIUM
Proprietary Name: CEFOTAXIME AND DEXTROSE 3.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N050792
Product Number: 002
Approval Date: Jul 29, 2004
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information