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Propafenone HCl - 63739-509-10 - (Propafenone hydrochloride)

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Drug Information of Propafenone HCl

Product NDC: 63739-509
Proprietary Name: Propafenone HCl
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 HCl

Product NDC: 63739-509
Labeler Name: McKesson Packaging Services a business unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075203
Marketing Category: ANDA
Start Marketing Date: 20120910

Package Information of Propafenone HCl

Package NDC: 63739-509-10
Package Description: 10 BLISTER PACK in 1 BOTTLE, UNIT-DOSE (63739-509-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Propafenone HCl

NDC Code 63739-509-10
Proprietary Name Propafenone HCl
Package Description 10 BLISTER PACK in 1 BOTTLE, UNIT-DOSE (63739-509-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 63739-509
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Propafenone hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120910
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services a business unit of McKesson Corporation
Substance Name PROPAFENONE HYDROCHLORIDE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of Propafenone HCl


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