Propafenone HCl

Product NDC
63739-510
11-digit product format
637390510
Labeler code
63739
Product ID
63739-510_36343a60-3d14-4748-b11f-379eec917b8c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Propafenone hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
McKesson Corporation dba SKY Packaging
Application
ANDA075203
Marketing category
ANDA
Marketing start
2000-10-24
Marketing end
0000-00-00
Substance
PROPAFENONE HYDROCHLORIDE
Active strength
225 mg/1
Pharmacologic classes
Antiarrhythmic [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63739-510-102020-07-22C16284748780-1ab0e2407-290e-f274-e053-dbdaa90a6471cf103bcc-5b96-4699-be2c-d596d490a814

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63739-510-10EA - Each63739-510ab872cd4-0f7f-4375-8860-00c8137adb4512013-02-13