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metoprolol succinate
metoprolol succinate - 58177-358-09 - (metoprolol succinate)
Drug Information of metoprolol succinate
| Product NDC: | 58177-358 |
| Proprietary Name: | metoprolol succinate |
| Non Proprietary Name: | metoprolol succinate |
| Active Ingredient(s): | 190 mg/1 & nbsp; metoprolol succinate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of metoprolol succinate
| Product NDC: | 58177-358 |
| Labeler Name: | Ethex Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076640 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091101 |
Package Information of metoprolol succinate
| Package NDC: | 58177-358-09 |
| Package Description: | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (58177-358-09) |
NDC Information of metoprolol succinate
| NDC Code | 58177-358-09 |
| Proprietary Name | metoprolol succinate |
| Package Description | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (58177-358-09) |
| Product NDC | 58177-358 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | metoprolol succinate |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20091101 |
| Marketing Category Name | ANDA |
| Labeler Name | Ethex Corporation |
| Substance Name | METOPROLOL SUCCINATE |
| Strength Number | 190 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
