| NDC Code: |
59762-0222 |
| Proprietary Name: |
quinapril hydrochloride and hydrochlorothiazide |
| Suffix: |
|
| Non-Proprietary Name: |
quinapril hydrochloride and hydrochlorothiazide |
| Dosage Form: |
TABLET, FILM COATED |
| Method: |
ORAL |
| Original Marketing Date: |
28-12-1999 |
| Category Name: |
NDA AUTHORIZED GENERIC |
| Application Number: |
NDA020125 |
| Labeler: |
GREENSTONE LLC |
| Substance Name: |
HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE |
| Active Numerator Strength: |
12.5; 10 |
| 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: |
|
