Product Details for NDA 019625
ELOCON (MOMETASONE FUROATE)
0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: MOMETASONE FUROATE
Proprietary Name: ELOCON
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: 0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N019625
Product Number: 001
Approval Date: May 6, 1987
Applicant Holder Full Name: ORGANON LLC A SUB OF ORGANON AND CO
Marketing Status: Discontinued
Patent and Exclusivity Information
ELOCON (MOMETASONE FUROATE)
Proprietary Name: ELOCON
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: 0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N019625
Product Number: 001
Approval Date: May 6, 1987
Applicant Holder Full Name: ORGANON LLC A SUB OF ORGANON AND CO
Marketing Status: Discontinued
Patent and Exclusivity Information
0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: MOMETASONE FUROATE
Proprietary Name: ELOCON
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: 0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N019625
Product Number: 002
Approval Date: Apr 19, 2013
Applicant Holder Full Name: ORGANON LLC A SUB OF ORGANON AND CO
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: ELOCON
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: 0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N019625
Product Number: 002
Approval Date: Apr 19, 2013
Applicant Holder Full Name: ORGANON LLC A SUB OF ORGANON AND CO
Marketing Status: Discontinued
Patent and Exclusivity Information