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Metoprolol Tartrate
Metoprolol Tartrate - 0781-3071-95 - (Metoprolol Tartrate)
Drug Information of Metoprolol Tartrate
| Product NDC: | 0781-3071 |
| Proprietary Name: | Metoprolol Tartrate |
| Non Proprietary Name: | Metoprolol Tartrate |
| Active Ingredient(s): | 5 mg/5mL & nbsp; Metoprolol Tartrate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Metoprolol Tartrate
| Product NDC: | 0781-3071 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077360 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20071002 |
Package Information of Metoprolol Tartrate
| Package NDC: | 0781-3071-95 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 CARTON (0781-3071-95) > 5 mL in 1 VIAL, SINGLE-DOSE (0781-3071-75) |
NDC Information of Metoprolol Tartrate
| NDC Code | 0781-3071-95 |
| Proprietary Name | Metoprolol Tartrate |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (0781-3071-95) > 5 mL in 1 VIAL, SINGLE-DOSE (0781-3071-75) |
| Product NDC | 0781-3071 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metoprolol Tartrate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20071002 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | METOPROLOL TARTRATE |
| Strength Number | 5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
