Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 070947

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PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE)
25MG;40MG
Marketing Status: Discontinued

Active Ingredient: HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
Proprietary Name: PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG;40MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A070947
Product Number: 002
Approval Date: Mar 4, 1987
Applicant Holder Full Name: RISING PHARMA HOLDINGS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE)
25MG;80MG
Marketing Status: Discontinued

Active Ingredient: HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
Proprietary Name: PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG;80MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A070947
Product Number: 001
Approval Date: Apr 1, 1987
Applicant Holder Full Name: RISING PHARMA HOLDINGS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information