Product NDC: | 52584-017 |
Proprietary Name: | Esmolol |
Non Proprietary Name: | Esmolol |
Active Ingredient(s): | 10 mg/mL & nbsp; Esmolol |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52584-017 |
Labeler Name: | General Injectables & Vaccines, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019386 |
Marketing Category: | NDA |
Start Marketing Date: | 20100401 |
Package NDC: | 52584-017-41 |
Package Description: | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-017-41) > 10 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 52584-017-41 |
Proprietary Name | Esmolol |
Package Description | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-017-41) > 10 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 52584-017 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Esmolol |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20100401 |
Marketing Category Name | NDA |
Labeler Name | General Injectables & Vaccines, Inc |
Substance Name | ESMOLOL HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |