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Amiodarone Hydrochloride - 55648-739-02 - (Amiodarone Hydrochloride)

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Drug Information of Amiodarone Hydrochloride

Product NDC: 55648-739
Proprietary Name: Amiodarone Hydrochloride
Non Proprietary Name: Amiodarone Hydrochloride
Active Ingredient(s): 50    mg/mL & nbsp;   Amiodarone Hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Amiodarone Hydrochloride

Product NDC: 55648-739
Labeler Name: Wockhardt Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077610
Marketing Category: ANDA
Start Marketing Date: 20081030

Package Information of Amiodarone Hydrochloride

Package NDC: 55648-739-02
Package Description: 10 VIAL in 1 CARTON (55648-739-02) > 3 mL in 1 VIAL

NDC Information of Amiodarone Hydrochloride

NDC Code 55648-739-02
Proprietary Name Amiodarone Hydrochloride
Package Description 10 VIAL in 1 CARTON (55648-739-02) > 3 mL in 1 VIAL
Product NDC 55648-739
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amiodarone Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20081030
Marketing Category Name ANDA
Labeler Name Wockhardt Limited
Substance Name AMIODARONE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of Amiodarone Hydrochloride


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