Amiloride Hydrochloride and Hydrochlorothiazide - amiloride hydrochloride and hydrochlorothiazide
Navigation: NDC > Supplier starting with: M > MYLAN PHARMACEUTICALS INC.| Field | Value |
|---|---|
| NDC Code: | 0378-0577 |
| Proprietary Name: | Amiloride Hydrochloride and Hydrochlorothiazide |
| Suffix: | |
| Non-Proprietary Name: | amiloride hydrochloride and hydrochlorothiazide |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 07-09-2011 |
| Category Name: | ANDA |
| Application Number: | ANDA073209 |
| Labeler: | MYLAN PHARMACEUTICALS INC. |
| Substance Name: | AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
| Active Numerator Strength: | 5; 50 |
| Active Ingredient Unit: | mg/1; mg/1 |
| Pharm Classes: | Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
| DEA Schedule: |