ELIQUIS

Product NDC
50090-6454
11-digit product format
500906454
Labeler code
50090
Product ID
50090-6454_d32cc824-92b9-4b7e-969f-181b7f5d815d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
apixaban
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
NDA202155
Marketing category
NDA
Marketing start
2012-12-28
Substance
APIXABAN
Active strength
5 mg/1
Pharmacologic classes
Factor Xa Inhibitor [EPC], Factor Xa 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
3Z9Y7UWC1JAPIXABAN503612-47-3APIXABAN

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
50090-6454-05009064540060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-6454-0) 2023-04-27NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
ELIQUISA-S Medication Solutions2023-05-09HUMAN PRESCRIPTION DRUG LABEL3