Warfarin Sodium

Product NDC
68788-7358
11-digit product format
687887358
Labeler code
68788
Product ID
68788-7358_510d1a24-563c-4e63-807f-c031fe44e39f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
warfarin sodium
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals, Inc.
Application
ANDA090935
Marketing category
ANDA
Marketing start
2011-11-11
Substance
WARFARIN SODIUM
Active strength
4 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

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
68788-7358-168788735801100 TABLET in 1 BOTTLE (68788-7358-1) 100 tablet2019-10-01NoNoHistorical
68788-7358-36878873580330 TABLET in 1 BOTTLE (68788-7358-3) 30 tablet2019-10-01NoNoHistorical
68788-7358-66878873580660 TABLET in 1 BOTTLE (68788-7358-6) 60 tablet2019-10-01NoNoHistorical
68788-7358-96878873580990 TABLET in 1 BOTTLE (68788-7358-9) 90 tablet2019-10-01NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Warfarin SodiumPreferred Pharmaceuticals, Inc.2025-10-08HUMAN PRESCRIPTION DRUG LABEL7
Warfarin SodiumPreferred Pharmaceuticals, Inc.2024-09-04HUMAN PRESCRIPTION DRUG LABEL6