Product NDC: | 67457-182 |
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) |
Product NDC: | 67457-182 |
Labeler Name: | Mylan Institutional LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076474 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130221 |
Package NDC: | 67457-182-10 |
Package Description: | 10 VIAL in 1 CARTON (67457-182-10) > 10 mL in 1 VIAL (67457-182-00) |
NDC Code | 67457-182-10 |
Proprietary Name | Esmolol Hydrochloride |
Package Description | 10 VIAL in 1 CARTON (67457-182-10) > 10 mL in 1 VIAL (67457-182-00) |
Product NDC | 67457-182 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | esmolol hydrochloride |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20130221 |
Marketing Category Name | ANDA |
Labeler Name | Mylan Institutional LLC |
Substance Name | ESMOLOL HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |