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Amiodarone Hydrochloride - 67457-153-03 - (amiodarone hydrochloride)

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Drug Information of Amiodarone Hydrochloride

Product NDC: 67457-153
Proprietary Name: Amiodarone Hydrochloride
Non Proprietary Name: amiodarone hydrochloride
Active Ingredient(s): 50    mg/mL & nbsp;   amiodarone hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Amiodarone Hydrochloride

Product NDC: 67457-153
Labeler Name: Mylan Institutional LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076217
Marketing Category: ANDA
Start Marketing Date: 20130604

Package Information of Amiodarone Hydrochloride

Package NDC: 67457-153-03
Package Description: 10 VIAL, GLASS in 1 CARTON (67457-153-03) > 3 mL in 1 VIAL, GLASS (67457-153-00)

NDC Information of Amiodarone Hydrochloride

NDC Code 67457-153-03
Proprietary Name Amiodarone Hydrochloride
Package Description 10 VIAL, GLASS in 1 CARTON (67457-153-03) > 3 mL in 1 VIAL, GLASS (67457-153-00)
Product NDC 67457-153
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amiodarone hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20130604
Marketing Category Name ANDA
Labeler Name Mylan Institutional LLC
Substance Name AMIODARONE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of Amiodarone Hydrochloride


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