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Metoprolol Tartrate
Metoprolol Tartrate - 0409-1778-05 - (METOPROLOL TARTRATE)
Drug Information of Metoprolol Tartrate
| Product NDC: | 0409-1778 |
| 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) |
Labeler Information of Metoprolol Tartrate
| Product NDC: | 0409-1778 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078085 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080429 |
Package Information of Metoprolol Tartrate
| Package NDC: | 0409-1778-05 |
| Package Description: | 10 VIAL, SINGLE-USE in 1 CARTON (0409-1778-05) > 5 mL in 1 VIAL, SINGLE-USE |
NDC Information of Metoprolol Tartrate
| NDC Code | 0409-1778-05 |
| Proprietary Name | Metoprolol Tartrate |
| Package Description | 10 VIAL, SINGLE-USE in 1 CARTON (0409-1778-05) > 5 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 0409-1778 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | METOPROLOL TARTRATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20080429 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | METOPROLOL TARTRATE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
