NDC Code | 68645-412-70 |
Package Description | 30 TABLET, FILM COATED in 1 DOSE PACK (68645-412-70) |
Product NDC | 68645-412 |
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 | Legacy Pharmaceutical Packaging |
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 [CS] |