Warfarin Sodium

Product NDC
0093-1719
11-digit product format
000931719
Labeler code
0093
Product ID
0093-1719_2dbc211e-8b33-466d-92cf-c7e56fe0b062
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Warfarin Sodium
Dosage form
TABLET
Route
ORAL
Labeler
Teva Pharmaceuticals USA, Inc.
Application
ANDA040616
Marketing category
ANDA
Marketing start
2015-06-09
Marketing end
2020-01-31
Substance
WARFARIN SODIUM
Active strength
8 mg/1
Pharmacologic classes
Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0093-1719-01EA - Each0093-171907b68b76-8e03-420d-a614-099aa11ac5f312015-07-20