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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 019304

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LIPIDIL (FENOFIBRATE)
100MG
Marketing Status: Discontinued
Active Ingredient: FENOFIBRATE
Proprietary Name: LIPIDIL
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019304
Product Number: 001
Approval Date: Dec 31, 1993
Applicant Holder Full Name: ABBVIE INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
TRICOR (MICRONIZED) (FENOFIBRATE)
67MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: FENOFIBRATE
Proprietary Name: TRICOR (MICRONIZED)
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 67MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N019304
Product Number: 002
Approval Date: Feb 9, 1998
Applicant Holder Full Name: ABBVIE INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
TRICOR (MICRONIZED) (FENOFIBRATE)
134MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: FENOFIBRATE
Proprietary Name: TRICOR (MICRONIZED)
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 134MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N019304
Product Number: 003
Approval Date: Jun 30, 1999
Applicant Holder Full Name: ABBVIE INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
TRICOR (MICRONIZED) (FENOFIBRATE)
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: FENOFIBRATE
Proprietary Name: TRICOR (MICRONIZED)
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N019304
Product Number: 004
Approval Date: Jun 30, 1999
Applicant Holder Full Name: ABBVIE INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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