| NDC Code: |
60505-2656 |
| Proprietary Name: |
Triamterene and Hydrochlorothiazide |
| Suffix: |
|
| Non-Proprietary Name: |
Triamterene and Hydrochlorothiazide |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
21-09-2009 |
| Category Name: |
ANDA |
| Application Number: |
ANDA071251 |
| Labeler: |
APOTEX CORP. |
| Substance Name: |
HYDROCHLOROTHIAZIDE; TRIAMTERENE |
| Active Numerator Strength: |
25; 37.5 |
| 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: |
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