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Amiodarone Hydrochloride - 76237-108-30 - (Amiodarone Hydrochloride)

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Drug Information of Amiodarone Hydrochloride

Product NDC: 76237-108
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: 76237-108
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075315
Marketing Category: ANDA
Start Marketing Date: 20120103

Package Information of Amiodarone Hydrochloride

Package NDC: 76237-108-30
Package Description: 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-108-30) > 5 TABLET in 1 BLISTER PACK

NDC Information of Amiodarone Hydrochloride

NDC Code 76237-108-30
Proprietary Name Amiodarone Hydrochloride
Package Description 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-108-30) > 5 TABLET in 1 BLISTER PACK
Product NDC 76237-108
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amiodarone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120103
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
Substance Name AMIODARONE HYDROCHLORIDE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of Amiodarone Hydrochloride


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