Digoxin

Product NDC
63629-3870
11-digit product format
636293870
Labeler code
63629
Product ID
63629-3870_badc96ff-8d82-49d8-929d-ee95c10abcf6
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Digoxin
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA077002
Marketing category
ANDA
Marketing start
2007-10-30
Marketing end
0000-00-00
Substance
DIGOXIN
Active strength
250 ug/1
Pharmacologic classes
Cardiac Glycoside [EPC],Cardiac Glycosides [CS]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-3870-1EA - Each63629-3870f2891189-ea71-4e7e-82c2-9bee668abae612013-02-13
63629-3870-2EA - Each63629-3870ea61a8f2-7a80-4217-b0be-20865dfb743812013-02-13
63629-3870-3EA - Each63629-3870af973162-003c-4ef2-9664-7bff958ccef212013-02-13
63629-3870-4EA - Each63629-38707b4a5d2b-8541-4e67-8f25-5ab71d85f83f12013-02-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-3870-16362938700130 TABLET in 1 BOTTLE (63629-3870-1) 30 tablet2008-10-310000-00-00NoNoCurrent
63629-3870-26362938700260 TABLET in 1 BOTTLE (63629-3870-2) 60 tablet2008-10-310000-00-00NoNoCurrent
63629-3870-36362938700390 TABLET in 1 BOTTLE (63629-3870-3) 90 tablet2008-10-310000-00-00NoNoCurrent
63629-3870-463629387004100 TABLET in 1 BOTTLE (63629-3870-4) 100 tablet2008-10-310000-00-00NoNoCurrent