| NDC Code: |
0781-5631 |
| Proprietary Name: |
Metoprolol Tartrate and Hydrochlorothiazide |
| Suffix: |
|
| Non-Proprietary Name: |
metoprolol tartrate and hydrochlorothiazide |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
01-12-1984 |
| End of Marketing: |
30-04-2014 |
| Category Name: |
NDA AUTHORIZED GENERIC |
| Application Number: |
NDA018303 |
| Labeler: |
SANDOZ INC |
| Substance Name: |
HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE |
| Active Numerator Strength: |
25; 100 |
| 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: |
|
