NDC Code |
65862-309-99 |
Proprietary Name |
Fosinopril Sodium and Hydrochlorothiazide |
Package Description |
1000 TABLET in 1 BOTTLE (65862-309-99) |
Product NDC |
65862-309 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
Fosinopril Sodium and Hydrochlorothiazide |
Dosage Form Name |
TABLET |
Route Name |
ORAL |
Start Marketing Date |
20090709 |
Marketing Category Name |
ANDA |
Labeler Name |
Aurobindo Pharma Limited |
Substance Name |
FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE |
Strength Number |
20; 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] |