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Amiodarone Hydrochloride - 60429-247-60 - (amiodarone hydrochloride)

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Drug Information of Amiodarone Hydrochloride

Product NDC: 60429-247
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: 60429-247
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075424
Marketing Category: ANDA
Start Marketing Date: 20010330

Package Information of Amiodarone Hydrochloride

Package NDC: 60429-247-60
Package Description: 60 TABLET in 1 BOTTLE (60429-247-60)

NDC Information of Amiodarone Hydrochloride

NDC Code 60429-247-60
Proprietary Name Amiodarone Hydrochloride
Package Description 60 TABLET in 1 BOTTLE (60429-247-60)
Product NDC 60429-247
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amiodarone hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010330
Marketing Category Name ANDA
Labeler Name Golden State Medical Supply, Inc.
Substance Name AMIODARONE HYDROCHLORIDE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of Amiodarone Hydrochloride


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