Lopressor HCT - metoprolol tartrate and hydrochlorothiazide
Navigation: NDC > Supplier starting with: N > NOVARTIS PHARMACEUTICALS CORPORATION| Field | Value |
|---|---|
| NDC Code: | 0078-0460 |
| Proprietary Name: | Lopressor HCT |
| Suffix: | |
| Non-Proprietary Name: | metoprolol tartrate and hydrochlorothiazide |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 01-12-1984 |
| End of Marketing: | 01-08-2014 |
| Category Name: | NDA |
| Application Number: | NDA018303 |
| Labeler: | NOVARTIS PHARMACEUTICALS CORPORATION |
| Substance Name: | HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE |
| Active Numerator Strength: | 25; 50 |
| 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: |