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TOPROL
TOPROL - 0186-1088-39 - (Metoprolol succinate)
Drug Information of TOPROL
| Product NDC: | 0186-1088 |
| Proprietary Name: | TOPROL |
| Non Proprietary Name: | Metoprolol succinate |
| Active Ingredient(s): | 25 mg/1 & nbsp; Metoprolol succinate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TOPROL
| Product NDC: | 0186-1088 |
| Labeler Name: | AstraZeneca LP |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019962 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20010326 |
Package Information of TOPROL
| Package NDC: | 0186-1088-39 |
| Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (0186-1088-39) |
NDC Information of TOPROL
| NDC Code | 0186-1088-39 |
| Proprietary Name | TOPROL |
| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (0186-1088-39) |
| Product NDC | 0186-1088 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metoprolol succinate |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20010326 |
| Marketing Category Name | NDA |
| Labeler Name | AstraZeneca LP |
| Substance Name | METOPROLOL SUCCINATE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
