NDC Code | 54569-5998-0 |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (54569-5998-0) |
Product NDC | 54569-5998 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Benicar Hct |
Non-Proprietary Name | Olmesartan Medoxomil-hydrochlorothiazide |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20030605 |
Marketing Category Name | NDA |
Application Number | NDA021532 |
Manufacturer | A-S Medication Solutions |
Substance Name | OLMESARTAN MEDOXOMIL; HYDROCHLOROTHIAZIDE |
Strength | 40; 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] |