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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 019451

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LOPRESSIDONE (CHLORTHALIDONE; METOPROLOL TARTRATE)
25MG;100MG
Marketing Status: Discontinued
Active Ingredient: CHLORTHALIDONE; METOPROLOL TARTRATE
Proprietary Name: LOPRESSIDONE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 25MG;100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019451
Product Number: 001
Approval Date: Dec 31, 1987
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information
LOPRESSIDONE (CHLORTHALIDONE; METOPROLOL TARTRATE)
25MG;200MG
Marketing Status: Discontinued
Active Ingredient: CHLORTHALIDONE; METOPROLOL TARTRATE
Proprietary Name: LOPRESSIDONE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 25MG;200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019451
Product Number: 002
Approval Date: Dec 31, 1987
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information
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