| NDC Code: |
0185-0701 |
| Proprietary Name: |
Bisoprolol Fumarate and Hydrochlorothiazide |
| Suffix: |
|
| Non-Proprietary Name: |
Bisoprolol Fumarate and Hydrochlorothiazide |
| Dosage Form: |
TABLET, COATED |
| Method: |
ORAL |
| Original Marketing Date: |
25-09-2000 |
| Category Name: |
ANDA |
| Application Number: |
ANDA075579 |
| Labeler: |
EON LABS, INC. |
| Substance Name: |
BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE |
| Active Numerator Strength: |
2.5; 6.25 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
| DEA Schedule: |
|
