| Product NDC: | 55154-5741 |
| Proprietary Name: | Metoprolol Tartrate |
| Non Proprietary Name: | Metoprolol Tartrate |
| Active Ingredient(s): | 1 mg/mL & nbsp; Metoprolol Tartrate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55154-5741 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090386 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100211 |
| Package NDC: | 55154-5741-5 |
| Package Description: | 5 VIAL, SINGLE-DOSE in 1 BAG (55154-5741-5) > 1 mL in 1 VIAL, SINGLE-DOSE |
| NDC Code | 55154-5741-5 |
| Proprietary Name | Metoprolol Tartrate |
| Package Description | 5 VIAL, SINGLE-DOSE in 1 BAG (55154-5741-5) > 1 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 55154-5741 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metoprolol Tartrate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20100211 |
| Marketing Category Name | ANDA |
| Labeler Name | Cardinal Health |
| Substance Name | METOPROLOL TARTRATE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |