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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 021350

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TRIGLIDE (FENOFIBRATE)
160MG
Marketing Status: Prescription
Active Ingredient: FENOFIBRATE
Proprietary Name: TRIGLIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 160MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: BX
Application Number: N021350
Product Number: 002
Approval Date: May 7, 2005
Applicant Holder Full Name: SKYEPHARMA AG
Marketing Status:  Prescription
Patent and Exclusivity Information
TRIGLIDE (FENOFIBRATE)
50MG
Marketing Status: Discontinued
Active Ingredient: FENOFIBRATE
Proprietary Name: TRIGLIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N021350
Product Number: 001
Approval Date: May 7, 2005
Applicant Holder Full Name: SKYEPHARMA AG
Marketing Status:  Discontinued
Patent and Exclusivity Information
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