Strength
25; 20 mg/1; mg/1
Manufacturer
Aurobindo Pharma LimitedNDC
65862016390
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
7/20/2022
Active Ingredients
HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA078450On Market Since
8/24/2007
Pharmacological Classes
Angiotensin Converting Enzyme Inhibitor
Angiotensin-converting Enzyme Inhibitors
Increased Diuresis
Thiazide Diuretic
Thiazides
Generic Alternatives
No alternatives available
No alternatives found with the same active ingredient, strength, and dosage form.
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