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PROPAFENONE HYDROCHLORIDE - 53489-551-10 - (propafenone hydrochloride)

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Drug Information of PROPAFENONE HYDROCHLORIDE

Product NDC: 53489-551
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: 53489-551
Labeler Name: Mutual Pharmaceutical Co., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075998
Marketing Category: ANDA
Start Marketing Date: 20011129

Package Information of PROPAFENONE HYDROCHLORIDE

Package NDC: 53489-551-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-551-10)

NDC Information of PROPAFENONE HYDROCHLORIDE

NDC Code 53489-551-10
Proprietary Name PROPAFENONE HYDROCHLORIDE
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-551-10)
Product NDC 53489-551
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name propafenone hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20011129
Marketing Category Name ANDA
Labeler Name Mutual Pharmaceutical Co., Inc.
Substance Name PROPAFENONE HYDROCHLORIDE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of PROPAFENONE HYDROCHLORIDE


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