Warfarin Sodium

Product NDC
71335-1824
11-digit product format
713351824
Labeler code
71335
Product ID
71335-1824_ad1f0082-5632-494c-9d30-7db1d8ebac02
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Warfarin
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA202202
Marketing category
ANDA
Marketing start
2010-08-16
Substance
WARFARIN SODIUM
Active strength
2.5 mg/1
Pharmacologic classes
Vitamin K Antagonist [EPC], Vitamin K Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
6153CWM0CLWARFARIN SODIUM129-06-6WARFARIN SODIUM
5Q7ZVV76EIWARFARIN81-81-2Warfarin

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-1824-17133518240130 TABLET in 1 BOTTLE (71335-1824-1) 30 tablet2021-12-21NoNoHistorical
71335-1824-27133518240260 TABLET in 1 BOTTLE (71335-1824-2) 60 tablet2021-12-21NoNoHistorical
71335-1824-37133518240315 TABLET in 1 BOTTLE (71335-1824-3) 15 tablet2021-12-21NoNoHistorical
71335-1824-47133518240490 TABLET in 1 BOTTLE (71335-1824-4) 90 tablet2021-12-21NoNoHistorical
71335-1824-571335182405100 TABLET in 1 BOTTLE (71335-1824-5) 100 tablet2021-12-21NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Warfarin SodiumBryant Ranch Prepack2023-10-20HUMAN PRESCRIPTION DRUG LABEL102