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METOPROLOL SUCCINATE
METOPROLOL SUCCINATE - 49884-407-01 - (Metoprolol succinate)
Drug Information of METOPROLOL SUCCINATE
| Product NDC: | 49884-407 |
| Proprietary Name: | METOPROLOL SUCCINATE |
| Non Proprietary Name: | Metoprolol succinate |
| Active Ingredient(s): | 200 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: | 49884-407 |
| Labeler Name: | Par Pharmaceutical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019962 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20070726 |
Package Information of METOPROLOL SUCCINATE
| Package NDC: | 49884-407-01 |
| Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (49884-407-01) |
NDC Information of METOPROLOL SUCCINATE
| NDC Code | 49884-407-01 |
| Proprietary Name | METOPROLOL SUCCINATE |
| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (49884-407-01) |
| Product NDC | 49884-407 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metoprolol succinate |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20070726 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Par Pharmaceutical Inc. |
| Substance Name | METOPROLOL SUCCINATE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
