Product Details for ANDA 065118
CEFUROXIME AXETIL (CEFUROXIME AXETIL)
EQ 125MG BASE
Marketing Status: Discontinued
EQ 250MG BASE
Marketing Status: Discontinued
EQ 500MG BASE
Marketing Status: Discontinued
EQ 125MG BASE
Marketing Status: Discontinued
Active Ingredient: CEFUROXIME AXETIL
Proprietary Name: CEFUROXIME AXETIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 125MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A065118
Product Number: 001
Approval Date: Apr 25, 2003
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
CEFUROXIME AXETIL (CEFUROXIME AXETIL)
Proprietary Name: CEFUROXIME AXETIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 125MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A065118
Product Number: 001
Approval Date: Apr 25, 2003
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 250MG BASE
Marketing Status: Discontinued
Active Ingredient: CEFUROXIME AXETIL
Proprietary Name: CEFUROXIME AXETIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 250MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A065118
Product Number: 002
Approval Date: Apr 25, 2003
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
CEFUROXIME AXETIL (CEFUROXIME AXETIL)
Proprietary Name: CEFUROXIME AXETIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 250MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A065118
Product Number: 002
Approval Date: Apr 25, 2003
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 500MG BASE
Marketing Status: Discontinued
Active Ingredient: CEFUROXIME AXETIL
Proprietary Name: CEFUROXIME AXETIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 500MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A065118
Product Number: 003
Approval Date: Apr 25, 2003
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: CEFUROXIME AXETIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 500MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A065118
Product Number: 003
Approval Date: Apr 25, 2003
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status: Discontinued
Patent and Exclusivity Information