Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 061049

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NEO-CORTEF (HYDROCORTISONE ACETATE; NEOMYCIN SULFATE)
1%;EQ 3.5MG BASE/GM
Marketing Status: Discontinued

Active Ingredient: HYDROCORTISONE ACETATE; NEOMYCIN SULFATE
Proprietary Name: NEO-CORTEF
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: 1%;EQ 3.5MG BASE/GM
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A061049
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status:  Discontinued
Patent and Exclusivity Information

NEO-CORTEF (HYDROCORTISONE ACETATE; NEOMYCIN SULFATE)
2.5%;EQ 3.5MG BASE/GM
Marketing Status: Discontinued

Active Ingredient: HYDROCORTISONE ACETATE; NEOMYCIN SULFATE
Proprietary Name: NEO-CORTEF
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: 2.5%;EQ 3.5MG BASE/GM
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A061049
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status:  Discontinued
Patent and Exclusivity Information