| NDC Code | 0378-1425-77 |
|---|
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-1425-77) |
|---|
| Product NDC | 0378-1425 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Olmesartan Medoxmil And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Olmesartan Medoxmil And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20161026 |
|---|
| End Marketing Date | 20191231 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078827 |
|---|
| Manufacturer | Mylan Pharmaceuticals Inc. |
|---|
| Substance Name | OLMESARTAN MEDOXOMIL; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 40; 25 |
|---|
| 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] |
|---|