Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

Home | Back to Search Results

Product Details for NDA 050672

Expand all

CEFTIN (CEFUROXIME AXETIL)
EQ 125MG BASE/5ML
Marketing Status: Discontinued

Active Ingredient: CEFUROXIME AXETIL
Proprietary Name: CEFTIN
Dosage Form; Route of Administration: FOR SUSPENSION; ORAL
Strength: EQ 125MG BASE/5ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N050672
Product Number: 001
Approval Date: Jun 30, 1994
Applicant Holder Full Name: GLAXOSMITHKLINE
Marketing Status:  Discontinued
Patent and Exclusivity Information

CEFTIN (CEFUROXIME AXETIL)
EQ 250MG BASE/5ML
Marketing Status: Discontinued

Active Ingredient: CEFUROXIME AXETIL
Proprietary Name: CEFTIN
Dosage Form; Route of Administration: FOR SUSPENSION; ORAL
Strength: EQ 250MG BASE/5ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N050672
Product Number: 002
Approval Date: Apr 29, 1997
Applicant Holder Full Name: GLAXOSMITHKLINE
Marketing Status:  Discontinued
Patent and Exclusivity Information