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Propafenone Hydrochloride - 49884-210-09 - (propafenone hydrochloride)

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Drug Information of Propafenone Hydrochloride

Product NDC: 49884-210
Proprietary Name: Propafenone Hydrochloride
Non Proprietary Name: propafenone hydrochloride
Active Ingredient(s): 325    mg/1 & nbsp;   propafenone hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Propafenone Hydrochloride

Product NDC: 49884-210
Labeler Name: Par Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078540
Marketing Category: ANDA
Start Marketing Date: 20110103

Package Information of Propafenone Hydrochloride

Package NDC: 49884-210-09
Package Description: 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49884-210-09)

NDC Information of Propafenone Hydrochloride

NDC Code 49884-210-09
Proprietary Name Propafenone Hydrochloride
Package Description 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49884-210-09)
Product NDC 49884-210
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name propafenone hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110103
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical, Inc.
Substance Name PROPAFENONE HYDROCHLORIDE
Strength Number 325
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of Propafenone Hydrochloride


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