Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 018031

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INDERIDE-40/25 (HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE)
25MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued

Active Ingredient: HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
Proprietary Name: INDERIDE-40/25
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N018031
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: WYETH PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

INDERIDE-80/25 (HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE)
25MG;80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued

Active Ingredient: HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
Proprietary Name: INDERIDE-80/25
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG;80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N018031
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: WYETH PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information