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Amiodarone Hydrochloride - 55390-105-01 - (Amiodarone Hydrochloride)

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Drug Information of Amiodarone Hydrochloride

Product NDC: 55390-105
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: 55390-105
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076299
Marketing Category: ANDA
Start Marketing Date: 20050906

Package Information of Amiodarone Hydrochloride

Package NDC: 55390-105-01
Package Description: 1 VIAL, MULTI-DOSE in 1 BOX (55390-105-01) > 9 mL in 1 VIAL, MULTI-DOSE

NDC Information of Amiodarone Hydrochloride

NDC Code 55390-105-01
Proprietary Name Amiodarone Hydrochloride
Package Description 1 VIAL, MULTI-DOSE in 1 BOX (55390-105-01) > 9 mL in 1 VIAL, MULTI-DOSE
Product NDC 55390-105
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amiodarone Hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20050906
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name AMIODARONE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of Amiodarone Hydrochloride


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