Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 075896

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FELODIPINE (FELODIPINE)
2.5MG
Marketing Status: Discontinued

Active Ingredient: FELODIPINE
Proprietary Name: FELODIPINE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 2.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A075896
Product Number: 001
Approval Date: Nov 2, 2004
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

FELODIPINE (FELODIPINE)
5MG
Marketing Status: Discontinued

Active Ingredient: FELODIPINE
Proprietary Name: FELODIPINE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A075896
Product Number: 002
Approval Date: Nov 2, 2004
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

FELODIPINE (FELODIPINE)
10MG
Marketing Status: Discontinued

Active Ingredient: FELODIPINE
Proprietary Name: FELODIPINE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A075896
Product Number: 003
Approval Date: Nov 2, 2004
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information