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Propafenone Hydrochloride - 0615-7574-39 - (Propafenone Hydrochloride)

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Drug Information of Propafenone Hydrochloride

Product NDC: 0615-7574
Proprietary Name: Propafenone Hydrochloride
Non Proprietary Name: Propafenone Hydrochloride
Active Ingredient(s): 150    mg/1 & nbsp;   Propafenone Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Propafenone Hydrochloride

Product NDC: 0615-7574
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075938
Marketing Category: ANDA
Start Marketing Date: 20021017

Package Information of Propafenone Hydrochloride

Package NDC: 0615-7574-39
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7574-39)

NDC Information of Propafenone Hydrochloride

NDC Code 0615-7574-39
Proprietary Name Propafenone Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7574-39)
Product NDC 0615-7574
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Propafenone Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20021017
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name PROPAFENONE HYDROCHLORIDE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of Propafenone Hydrochloride


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