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TOPROL
TOPROL - 54868-3587-0 - (Metoprolol succinate)
Drug Information of TOPROL
| Product NDC: | 54868-3587 |
| Proprietary Name: | TOPROL |
| Non Proprietary Name: | Metoprolol succinate |
| Active Ingredient(s): | 50 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: | 54868-3587 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019962 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030709 |
Package Information of TOPROL
| Package NDC: | 54868-3587-0 |
| Package Description: | 50 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-3587-0) |
NDC Information of TOPROL
| NDC Code | 54868-3587-0 |
| Proprietary Name | TOPROL |
| Package Description | 50 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-3587-0) |
| Product NDC | 54868-3587 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metoprolol succinate |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20030709 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | METOPROLOL SUCCINATE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
