RYTHMOL - 0173-0826-18 - (propafenone hydrochloride)

Alphabetical Index


Drug Information of RYTHMOL

Product NDC: 0173-0826
Proprietary Name: RYTHMOL
Non Proprietary Name: propafenone hydrochloride
Active Ingredient(s): 425    mg/1 & nbsp;   propafenone hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of RYTHMOL

Product NDC: 0173-0826
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021416
Marketing Category: NDA
Start Marketing Date: 20110317

Package Information of RYTHMOL

Package NDC: 0173-0826-18
Package Description: 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0173-0826-18)

NDC Information of RYTHMOL

NDC Code 0173-0826-18
Proprietary Name RYTHMOL
Package Description 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0173-0826-18)
Product NDC 0173-0826
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name propafenone hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110317
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name PROPAFENONE HYDROCHLORIDE
Strength Number 425
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of RYTHMOL


General Information