Product Details for ANDA 065517
CEFOTAXIME SODIUM (CEFOTAXIME SODIUM)
EQ 500MG BASE/VIAL
Marketing Status: Discontinued
EQ 1GM BASE/VIAL
Marketing Status: Discontinued
EQ 2GM BASE/VIAL
Marketing Status: Discontinued
EQ 500MG BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: CEFOTAXIME SODIUM
Proprietary Name: CEFOTAXIME SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 500MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A065517
Product Number: 001
Approval Date: Nov 6, 2009
Applicant Holder Full Name: AUROBINDO PHARMA LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
CEFOTAXIME SODIUM (CEFOTAXIME SODIUM)
Proprietary Name: CEFOTAXIME SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 500MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A065517
Product Number: 001
Approval Date: Nov 6, 2009
Applicant Holder Full Name: AUROBINDO PHARMA LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 1GM BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: CEFOTAXIME SODIUM
Proprietary Name: CEFOTAXIME SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A065517
Product Number: 002
Approval Date: Nov 6, 2009
Applicant Holder Full Name: AUROBINDO PHARMA LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
CEFOTAXIME SODIUM (CEFOTAXIME SODIUM)
Proprietary Name: CEFOTAXIME SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A065517
Product Number: 002
Approval Date: Nov 6, 2009
Applicant Holder Full Name: AUROBINDO PHARMA LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 2GM BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: CEFOTAXIME SODIUM
Proprietary Name: CEFOTAXIME SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 2GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A065517
Product Number: 003
Approval Date: Nov 6, 2009
Applicant Holder Full Name: AUROBINDO PHARMA LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: CEFOTAXIME SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 2GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A065517
Product Number: 003
Approval Date: Nov 6, 2009
Applicant Holder Full Name: AUROBINDO PHARMA LTD
Marketing Status: Discontinued
Patent and Exclusivity Information