Losartan Potassium and Hydrochlorothiazide - losartan potassium and hydrochlorothiazide
Navigation: NDC > Supplier starting with: M > MYLAN PHARMACEUTICALS INC.| Field | Value |
|---|---|
| NDC Code: | 0378-1419 |
| Proprietary Name: | Losartan Potassium and Hydrochlorothiazide |
| Suffix: | |
| Non-Proprietary Name: | losartan potassium and hydrochlorothiazide |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 05-10-2012 |
| Category Name: | ANDA |
| Application Number: | ANDA091652 |
| Labeler: | MYLAN PHARMACEUTICALS INC. |
| Substance Name: | HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM |
| Active Numerator Strength: | 12.5; 100 |
| Active Ingredient Unit: | mg/1; mg/1 |
| Pharm Classes: | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
| DEA Schedule: |