NDC Code |
0378-0544-93 |
Proprietary Name |
Quinapril Hydrochloride and Hydrochlorothiazide |
Package Description |
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0544-93) |
Product NDC |
0378-0544 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
quinapril hydrochloride and hydrochlorothiazide |
Dosage Form Name |
TABLET, FILM COATED |
Route Name |
ORAL |
Start Marketing Date |
20121018 |
Marketing Category Name |
ANDA |
Labeler Name |
Mylan Pharmaceuticals Inc. |
Substance Name |
HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE |
Strength Number |
25; 20 |
Strength Unit |
mg/1; mg/1 |
Pharmaceutical Classes |
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |