Active Ingredient: CEFACLOR
Proprietary Name: CECLOR CD
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: EQ 375MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050673
Product Number: 001
Approval Date: Jun 28, 1996
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status:
Discontinued
Patent and Exclusivity Information
Active Ingredient: CEFACLOR
Proprietary Name: CECLOR CD
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050673
Product Number: 002
Approval Date: Jun 28, 1996
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status:
Discontinued
Patent and Exclusivity Information