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Esmolol Hydrochloride - 67457-182-10 - (esmolol hydrochloride)

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Drug Information of Esmolol Hydrochloride

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)

Labeler Information of Esmolol Hydrochloride

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 Information of Esmolol Hydrochloride

Package NDC: 67457-182-10
Package Description: 10 VIAL in 1 CARTON (67457-182-10) > 10 mL in 1 VIAL (67457-182-00)

NDC Information of Esmolol Hydrochloride

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]

Complete Information of Esmolol Hydrochloride


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