Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 050440

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KEFLET (CEPHALEXIN)
EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued

Active Ingredient: CEPHALEXIN
Proprietary Name: KEFLET
Dosage Form; Route of Administration: TABLET; 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Strength: EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N050440
Product Number: 003
Approval Date: Feb 26, 1987
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status:  Discontinued
Patent and Exclusivity Information

KEFLET (CEPHALEXIN)
EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued

Active Ingredient: CEPHALEXIN
Proprietary Name: KEFLET
Dosage Form; Route of Administration: TABLET; 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Strength: EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N050440
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

KEFLET (CEPHALEXIN)
EQ 1GM BASE
Marketing Status: Discontinued

Active Ingredient: CEPHALEXIN
Proprietary Name: KEFLET
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 1GM BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N050440
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