Warfarin Sodium

Product NDC
68788-7357
11-digit product format
687887357
Labeler code
68788
Product ID
68788-7357_119944bd-6e8b-4f98-bb7d-9aba0b9cd92e
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
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

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
68788-7357-168788735701100 TABLET in 1 BOTTLE (68788-7357-1) 100 tablet2019-09-27NoNoHistorical
68788-7357-36878873570330 TABLET in 1 BOTTLE (68788-7357-3) 30 tablet2019-09-27NoNoHistorical
68788-7357-66878873570660 TABLET in 1 BOTTLE (68788-7357-6) 60 tablet2019-09-27NoNoHistorical
68788-7357-96878873570990 TABLET in 1 BOTTLE (68788-7357-9) 90 tablet2019-09-27NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Warfarin SodiumPreferred Pharmaceuticals, Inc.2025-10-07HUMAN PRESCRIPTION DRUG LABEL7
Warfarin SodiumPreferred Pharmaceuticals, Inc.2024-09-04HUMAN PRESCRIPTION DRUG LABEL6