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Amiodarone Hydrochloride - 55154-5492-0 - (Amiodarone Hydrochloride)

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Drug Information of Amiodarone Hydrochloride

Product NDC: 55154-5492
Proprietary Name: Amiodarone Hydrochloride
Non Proprietary Name: Amiodarone Hydrochloride
Active Ingredient(s): 200    mg/1 & nbsp;   Amiodarone Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Amiodarone Hydrochloride

Product NDC: 55154-5492
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074739
Marketing Category: ANDA
Start Marketing Date: 19981130

Package Information of Amiodarone Hydrochloride

Package NDC: 55154-5492-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5492-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Amiodarone Hydrochloride

NDC Code 55154-5492-0
Proprietary Name Amiodarone Hydrochloride
Package Description 10 BLISTER PACK in 1 BAG (55154-5492-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-5492
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amiodarone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19981130
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name AMIODARONE HYDROCHLORIDE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of Amiodarone Hydrochloride


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