| NDC Code: |
0555-0483 |
| Proprietary Name: |
Amiloride Hydrochloride and Hydrochlorothiazide |
| Suffix: |
|
| Non-Proprietary Name: |
Amiloride Hydrochloride and Hydrochlorothiazide |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
01-12-1989 |
| Category Name: |
ANDA |
| Application Number: |
ANDA071111 |
| Labeler: |
BARR LABORATORIES 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: |
|
