| NDC Code: |
59762-5251 |
| Proprietary Name: |
Fosinopril Sodium and Hydrochlorothiazide |
| Suffix: |
|
| Non-Proprietary Name: |
Fosinopril Sodium and Hydrochlorothiazide |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
09-07-2009 |
| Category Name: |
ANDA |
| Application Number: |
ANDA079245 |
| Labeler: |
GREENSTONE LLC |
| Substance Name: |
FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE |
| Active Numerator Strength: |
20; 12.5 |
| 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: |
|
