Product Details for NDA 011835
HYDRODIURIL (HYDROCHLOROTHIAZIDE)
25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: HYDROCHLOROTHIAZIDE
Proprietary Name: HYDRODIURIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N011835
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status: Discontinued
Patent and Exclusivity Information
HYDRODIURIL (HYDROCHLOROTHIAZIDE)
Proprietary Name: HYDRODIURIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N011835
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status: Discontinued
Patent and Exclusivity Information
50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: HYDROCHLOROTHIAZIDE
Proprietary Name: HYDRODIURIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N011835
Product Number: 006
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status: Discontinued
Patent and Exclusivity Information
HYDRODIURIL (HYDROCHLOROTHIAZIDE)
Proprietary Name: HYDRODIURIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG **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: N011835
Product Number: 006
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status: Discontinued
Patent and Exclusivity Information
100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: HYDROCHLOROTHIAZIDE
Proprietary Name: HYDRODIURIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG **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: N011835
Product Number: 007
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: HYDRODIURIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG **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: N011835
Product Number: 007
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status: Discontinued
Patent and Exclusivity Information