| NDC Code | 35356-257-90 |
|---|
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (35356-257-90) |
|---|
| Product NDC | 35356-257 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Benicar Hct |
|---|
| Non-Proprietary Name | Olmesartan Medoxomil And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20120222 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA021532 |
|---|
| Manufacturer | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
|---|
| 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] |
|---|