Product Details for NDA 021203
TRICOR (FENOFIBRATE)
54MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
54MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: FENOFIBRATE
Proprietary Name: TRICOR
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 54MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N021203
Product Number: 001
Approval Date: Sep 4, 2001
Applicant Holder Full Name: ABBVIE INC
Marketing Status: Discontinued
Patent and Exclusivity Information
TRICOR (FENOFIBRATE)
Proprietary Name: TRICOR
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 54MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N021203
Product Number: 001
Approval Date: Sep 4, 2001
Applicant Holder Full Name: ABBVIE INC
Marketing Status: Discontinued
Patent and Exclusivity Information
160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: FENOFIBRATE
Proprietary Name: TRICOR
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N021203
Product Number: 003
Approval Date: Sep 4, 2001
Applicant Holder Full Name: ABBVIE INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: TRICOR
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N021203
Product Number: 003
Approval Date: Sep 4, 2001
Applicant Holder Full Name: ABBVIE INC
Marketing Status: Discontinued
Patent and Exclusivity Information