Product Details for NDA 050521
CECLOR (CEFACLOR)
EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: CEFACLOR
Proprietary Name: CECLOR
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N050521
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status: Discontinued
Patent and Exclusivity Information
CECLOR (CEFACLOR)
Proprietary Name: CECLOR
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N050521
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: CEFACLOR
Proprietary Name: CECLOR
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N050521
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: CECLOR
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N050521
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status: Discontinued
Patent and Exclusivity Information