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Amiodarone HCl - 51862-156-30 - (Amiodarone Hydrochloride)

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Drug Information of Amiodarone HCl

Product NDC: 51862-156
Proprietary Name: Amiodarone HCl
Non Proprietary Name: Amiodarone Hydrochloride
Active Ingredient(s): 400    mg/1 & nbsp;   Amiodarone Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Amiodarone HCl

Product NDC: 51862-156
Labeler Name: Libertas Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077069
Marketing Category: ANDA
Start Marketing Date: 20130101

Package Information of Amiodarone HCl

Package NDC: 51862-156-30
Package Description: 30 TABLET in 1 BOTTLE (51862-156-30)

NDC Information of Amiodarone HCl

NDC Code 51862-156-30
Proprietary Name Amiodarone HCl
Package Description 30 TABLET in 1 BOTTLE (51862-156-30)
Product NDC 51862-156
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amiodarone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130101
Marketing Category Name ANDA
Labeler Name Libertas Pharma, Inc.
Substance Name AMIODARONE HYDROCHLORIDE
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of Amiodarone HCl


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