Product Details for NDA 016908
LIDEX (FLUOCINONIDE)
0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: FLUOCINONIDE
Proprietary Name: LIDEX
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N016908
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ALVOGEN INC
Marketing Status: Discontinued
Patent and Exclusivity Information
LIDEX-E (FLUOCINONIDE)
Proprietary Name: LIDEX
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N016908
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ALVOGEN INC
Marketing Status: Discontinued
Patent and Exclusivity Information
0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: FLUOCINONIDE
Proprietary Name: LIDEX-E
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N016908
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ALVOGEN INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: LIDEX-E
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N016908
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ALVOGEN INC
Marketing Status: Discontinued
Patent and Exclusivity Information