| NDC Code | 60505-2915-0 |
|---|
| Package Description | 10 BLISTER PACK in 1 CARTON (60505-2915-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
|---|
| Product NDC | 60505-2915 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Losartan Potassium And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Losartan Potassium And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20101006 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090150 |
|---|
| Manufacturer | Apotex Corp. |
|---|
| Substance Name | LOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 50; 12.5 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
|---|