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Metoprolol
Metoprolol - 63323-660-05 - (METOPROLOL TARTRATE)
Drug Information of Metoprolol
| Product NDC: | 63323-660 |
| Proprietary Name: | Metoprolol |
| 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
| Product NDC: | 63323-660 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091045 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101028 |
Package Information of Metoprolol
| Package NDC: | 63323-660-05 |
| Package Description: | 10 VIAL in 1 TRAY (63323-660-05) > 5 mL in 1 VIAL |
NDC Information of Metoprolol
| NDC Code | 63323-660-05 |
| Proprietary Name | Metoprolol |
| Package Description | 10 VIAL in 1 TRAY (63323-660-05) > 5 mL in 1 VIAL |
| Product NDC | 63323-660 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | METOPROLOL TARTRATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20101028 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | METOPROLOL TARTRATE |
| Strength Number | 5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
