| NDC Code |
51079-757-20 |
| Proprietary Name |
Losartan Potassium and Hydrochlorothiazide |
| 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 |
| Non Proprietary Name |
losartan potassium and hydrochlorothiazide |
| Dosage Form Name |
TABLET, FILM COATED |
| Route Name |
ORAL |
| Start Marketing Date |
20111006 |
| Marketing Category Name |
ANDA |
| Labeler Name |
UDL Laboratories, Inc. |
| Substance Name |
HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM |
| Strength Number |
12.5; 50 |
| Strength Unit |
mg/1; mg/1 |
| Pharmaceutical Classes |
Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |