NDC Code |
23155-060-03 |
Proprietary Name |
Fosinopril Sodium and Hydrochlorothiazide |
Package Description |
30 TABLET in 1 BOTTLE (23155-060-03) |
Product NDC |
23155-060 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
Fosinopril Sodium and Hydrochlorothiazide Tablet |
Dosage Form Name |
TABLET |
Route Name |
ORAL |
Start Marketing Date |
20111115 |
Marketing Category Name |
ANDA |
Labeler Name |
Heritage Pharmaceuticals Inc. |
Substance Name |
FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE |
Strength Number |
10; 12.5 |
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] |