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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 062549

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KEFLIN IN PLASTIC CONTAINER (CEPHALOTHIN SODIUM)
EQ 1GM BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: CEPHALOTHIN SODIUM
Proprietary Name: KEFLIN IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A062549
Product Number: 001
Approval Date: Sep 10, 1985
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status:  Discontinued
Patent and Exclusivity Information
KEFLIN IN PLASTIC CONTAINER (CEPHALOTHIN SODIUM)
EQ 2GM BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: CEPHALOTHIN SODIUM
Proprietary Name: KEFLIN IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 2GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A062549
Product Number: 002
Approval Date: Sep 10, 1985
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status:  Discontinued
Patent and Exclusivity Information
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