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Amiodarone hydrochloride - 21695-796-30 - (Amiodarone hydrochloride)

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Drug Information of Amiodarone hydrochloride

Product NDC: 21695-796
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: 21695-796
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079029
Marketing Category: ANDA
Start Marketing Date: 20090810

Package Information of Amiodarone hydrochloride

Package NDC: 21695-796-30
Package Description: 30 TABLET in 1 BOTTLE (21695-796-30)

NDC Information of Amiodarone hydrochloride

NDC Code 21695-796-30
Proprietary Name Amiodarone hydrochloride
Package Description 30 TABLET in 1 BOTTLE (21695-796-30)
Product NDC 21695-796
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amiodarone hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090810
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name AMIODARONE HYDROCHLORIDE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of Amiodarone hydrochloride


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