Warfarin Sodium

Product NDC
68788-7515
11-digit product format
687887515
Labeler code
68788
Product ID
68788-7515_8dcd0b90-0188-40c9-9b60-e00932ae21c6
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 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

Additional Listing Data#

Finished product
Yes
Brand name base
Warfarin Sodium
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
WARFARIN SODIUM2 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii6153CWM0CL
Rxcui855302

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68788-7515-168788751501100 TABLET in 1 BOTTLE (68788-7515-1) 100 tablet2019-11-300000-00-00NoNoCurrent
68788-7515-36878875150330 TABLET in 1 BOTTLE (68788-7515-3) 30 tablet2019-11-300000-00-00NoNoCurrent
68788-7515-66878875150660 TABLET in 1 BOTTLE (68788-7515-6) 60 tablet2019-11-300000-00-00NoNoCurrent
68788-7515-96878875150990 TABLET in 1 BOTTLE (68788-7515-9) 90 tablet2019-11-300000-00-00NoNoCurrent