NDC Code | 43063-986-30 |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-986-30) |
Product NDC | 43063-986 |
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 | ANDA091629 |
Manufacturer | PD-Rx Pharmaceuticals, 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 [CS] |