| NDC Code: |
16714-417 |
| Proprietary Name: |
Metoprolol Tartrate and Hydrochlorothiazide |
| Suffix: |
50 mg-25 mg |
| Non-Proprietary Name: |
Metoprolol Tartrate and Hydrochlorothiazide |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
17-09-2013 |
| Category Name: |
ANDA |
| Application Number: |
ANDA202870 |
| Labeler: |
NORTHSTAR RXLLC |
| Substance Name: |
HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE |
| Active Numerator Strength: |
25; 50 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
| DEA Schedule: |
|
