Esmolol - 52584-017-41 - (Esmolol)

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Drug Information of Esmolol

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)

Labeler Information of Esmolol

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 Information of Esmolol

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 Information of Esmolol

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]

Complete Information of Esmolol


General Information