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Esmolol Hydrochloride
Esmolol Hydrochloride - 55390-062-10 - (Esmolol Hydrochloride)
Drug Information of Esmolol Hydrochloride
| Product NDC: | 55390-062 |
| Proprietary Name: | Esmolol Hydrochloride |
| Non Proprietary Name: | Esmolol Hydrochloride |
| Active Ingredient(s): | 10 mg/mL & nbsp; Esmolol Hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Esmolol Hydrochloride
| Product NDC: | 55390-062 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076323 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20041004 |
Package Information of Esmolol Hydrochloride
| Package NDC: | 55390-062-10 |
| Package Description: | 10 VIAL in 1 BOX (55390-062-10) > 10 mL in 1 VIAL |
NDC Information of Esmolol Hydrochloride
| NDC Code | 55390-062-10 |
| Proprietary Name | Esmolol Hydrochloride |
| Package Description | 10 VIAL in 1 BOX (55390-062-10) > 10 mL in 1 VIAL |
| Product NDC | 55390-062 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Esmolol Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20041004 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | ESMOLOL HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
