| NDC Code | 51079-757-20 |
|---|
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-757-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-757-01) |
|---|
| Product NDC | 51079-757 |
|---|
| 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 | 20111006 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA091652 |
|---|
| Manufacturer | UDL Laboratories, Inc. |
|---|
| Substance Name | HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM |
|---|
| Strength | 12.5; 50 |
|---|
| 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] |
|---|