NDC Code: |
60505-3411 |
Proprietary Name: |
Quinapril Hydrochloride and Hydrochlorothiazide |
Suffix: |
|
Non-Proprietary Name: |
Quinapril Hydrochloride and Hydrochlorothiazide |
Dosage Form: |
TABLET, FILM COATED |
Method: |
ORAL |
Original Marketing Date: |
12-03-2013 |
Category Name: |
ANDA |
Application Number: |
ANDA091524 |
Labeler: |
APOTEX CORP |
Substance Name: |
HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE |
Active Numerator Strength: |
25; 20 |
Active Ingredient Unit: |
mg/1; mg/1 |
Pharm Classes: |
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
DEA Schedule: |
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