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Esmolol Hydrochloride - 55390-062-10 - (Esmolol Hydrochloride)

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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]

Complete Information of Esmolol Hydrochloride


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