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Dutoprol
Dutoprol - 0310-1087-30 - (metoprolol succinate and hydrochlorothiazide)
Drug Information of Dutoprol
| Product NDC: | 0310-1087 |
| Proprietary Name: | Dutoprol |
| Non Proprietary Name: | metoprolol succinate and hydrochlorothiazide |
| Active Ingredient(s): | 12.5; 25 mg/1; mg/1 & nbsp; metoprolol succinate and hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dutoprol
| Product NDC: | 0310-1087 |
| Labeler Name: | AstraZeneca Pharmaceuticals LP |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021956 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20111230 |
Package Information of Dutoprol
| Package NDC: | 0310-1087-30 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (0310-1087-30) |
NDC Information of Dutoprol
| NDC Code | 0310-1087-30 |
| Proprietary Name | Dutoprol |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (0310-1087-30) |
| Product NDC | 0310-1087 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | metoprolol succinate and hydrochlorothiazide |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20111230 |
| Marketing Category Name | NDA |
| Labeler Name | AstraZeneca Pharmaceuticals LP |
| Substance Name | HYDROCHLOROTHIAZIDE; METOPROLOL SUCCINATE |
| Strength Number | 12.5; 25 |
| 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] |
