Home
>
National Drug Code (NDC)
>
Metoprolol succinate
Metoprolol succinate - 55111-468-78 - (Metoprolol succinate)
Drug Information of Metoprolol succinate
| Product NDC: | 55111-468 |
| Proprietary Name: | Metoprolol succinate |
| Non Proprietary Name: | Metoprolol succinate |
| Active Ingredient(s): | 100 mg/1 & nbsp; Metoprolol succinate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Metoprolol succinate
| Product NDC: | 55111-468 |
| Labeler Name: | Dr. Reddy's Laboratories Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078889 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120910 |
Package Information of Metoprolol succinate
| Package NDC: | 55111-468-78 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (55111-468-78) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (55111-468-79) |
NDC Information of Metoprolol succinate
| NDC Code | 55111-468-78 |
| Proprietary Name | Metoprolol succinate |
| Package Description | 10 BLISTER PACK in 1 CARTON (55111-468-78) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (55111-468-79) |
| Product NDC | 55111-468 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metoprolol succinate |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120910 |
| Marketing Category Name | ANDA |
| Labeler Name | Dr. Reddy's Laboratories Limited |
| Substance Name | METOPROLOL SUCCINATE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
