Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 019001

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BEPADIN (BEPRIDIL HYDROCHLORIDE)
200MG
Marketing Status: Discontinued

Active Ingredient: BEPRIDIL HYDROCHLORIDE
Proprietary Name: BEPADIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019001
Product Number: 001
Approval Date: Dec 28, 1990
Applicant Holder Full Name: MEDPOINTE PHARMACEUTICALS MEDPOINTE HEALTHCARE INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

BEPADIN (BEPRIDIL HYDROCHLORIDE)
300MG
Marketing Status: Discontinued

Active Ingredient: BEPRIDIL HYDROCHLORIDE
Proprietary Name: BEPADIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 300MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019001
Product Number: 002
Approval Date: Dec 28, 1990
Applicant Holder Full Name: MEDPOINTE PHARMACEUTICALS MEDPOINTE HEALTHCARE INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

BEPADIN (BEPRIDIL HYDROCHLORIDE)
400MG
Marketing Status: Discontinued

Active Ingredient: BEPRIDIL HYDROCHLORIDE
Proprietary Name: BEPADIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 400MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019001
Product Number: 003
Approval Date: Dec 28, 1990
Applicant Holder Full Name: MEDPOINTE PHARMACEUTICALS MEDPOINTE HEALTHCARE INC
Marketing Status:  Discontinued
Patent and Exclusivity Information