Home
>
National Drug Code (NDC)
>
Metoprolol Tartrate and Hydrochlorothiazide
Metoprolol Tartrate and Hydrochlorothiazide - 0781-5631-01 - (metoprolol tartrate and hydrochlorothiazide)
Drug Information of Metoprolol Tartrate and Hydrochlorothiazide
| Product NDC: | 0781-5631 |
| Proprietary Name: | Metoprolol Tartrate and Hydrochlorothiazide |
| Non Proprietary Name: | metoprolol tartrate and hydrochlorothiazide |
| Active Ingredient(s): | 25; 100 mg/1; mg/1 & nbsp; metoprolol tartrate and hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Metoprolol Tartrate and Hydrochlorothiazide
| Product NDC: | 0781-5631 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018303 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19841201 |
Package Information of Metoprolol Tartrate and Hydrochlorothiazide
| Package NDC: | 0781-5631-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0781-5631-01) |
NDC Information of Metoprolol Tartrate and Hydrochlorothiazide
| NDC Code | 0781-5631-01 |
| Proprietary Name | Metoprolol Tartrate and Hydrochlorothiazide |
| Package Description | 100 TABLET in 1 BOTTLE (0781-5631-01) |
| Product NDC | 0781-5631 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | metoprolol tartrate and hydrochlorothiazide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19841201 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Sandoz Inc |
| Substance Name | HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE |
| Strength Number | 25; 100 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
