Warfarin Sodium

Product NDC
50090-5439
11-digit product format
500905439
Labeler code
50090
Product ID
50090-5439_0ab1fd84-65f5-471a-8482-639e657aa1cc
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Warfarin Sodium
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA040616
Marketing category
ANDA
Marketing start
2015-04-07
Marketing end
0000-00-00
Substance
WARFARIN SODIUM
Active strength
5 mg/1
Pharmacologic classes
Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2022-12-31
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
50090-5439-0EA - Each50090-543932b105a7-e113-46de-a58b-0b437e4c1c0f12023-10-16
50090-5439-1EA - Each50090-543988c68ebd-007e-4258-9431-3d5c326d2e2d12023-10-16
50090-5439-2EA - Each50090-543999347fa3-2136-4044-9a71-5c1d8a373db012023-10-16

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-5439-05009054390030 TABLET in 1 BOTTLE (50090-5439-0) 30 tablet2021-01-200000-00-00NoNoCurrent
50090-5439-15009054390160 TABLET in 1 BOTTLE (50090-5439-1) 60 tablet2019-05-310000-00-00NoNoCurrent
50090-5439-25009054390290 TABLET in 1 BOTTLE (50090-5439-2) 90 tablet2021-01-200000-00-00NoNoCurrent