metoprolol succinate and hydrochlorothiazide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Solubiomix. The primary component is Metoprolol Succinate; Hydrochlorothiazide.
Product ID | 69499-323_882300e1-5fa3-4637-aa5f-6156209bd1c3 |
NDC | 69499-323 |
Product Type | Human Prescription Drug |
Proprietary Name | metoprolol succinate and hydrochlorothiazide |
Generic Name | Metoprolol Succinate And Hydrochlorothiazide |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2017-05-10 |
Marketing Category | NDA / NDA |
Application Number | NDA021956 |
Labeler Name | Solubiomix |
Substance Name | METOPROLOL SUCCINATE; HYDROCHLOROTHIAZIDE |
Active Ingredient Strength | 50 mg/1; mg/1 |
Pharm Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2017-05-10 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA021956 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2017-05-10 |
Marketing End Date | 2019-12-31 |
Ingredient | Strength |
---|---|
METOPROLOL SUCCINATE | 50 mg/1 |
SPL SET ID: | 20c2caf9-4c2e-42ac-b02c-f220893ec5a1 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
69499-321 | metoprolol succinate and hydrochlorothiazide | metoprolol succinate and hydrochlorothiazide |
69499-323 | metoprolol succinate and hydrochlorothiazide | metoprolol succinate and hydrochlorothiazide |
69499-324 | metoprolol succinate and hydrochlorothiazide | metoprolol succinate and hydrochlorothiazide |
59212-087 | Dutoprol | metoprolol succinate and hydrochlorothiazide |
59212-095 | Dutoprol | metoprolol succinate and hydrochlorothiazide |
59212-097 | Dutoprol | metoprolol succinate and hydrochlorothiazide |