NDC 0003-0894 – Eliquis

Apixaban 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC0003-0894

Product details

Brand name
Eliquis
Generic name
Apixaban
Labeler
E.R. Squibb & Sons, L.L.C.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA202155
Marketed since
December 28, 2012
Listing expires
December 31, 2027
Pharmacologic class
Factor Xa Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Eliquis →

Package NDC codes (4)

Package NDCDescriptionSince
0003-0894-2160 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0003-0894-21)Dec 28, 2012
0003-0894-3110 BLISTER PACK in 1 CARTON (0003-0894-31) / 10 TABLET, FILM COATED in 1 BLISTER PACKDec 28, 2012
0003-0894-7074 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0003-0894-70)Jun 1, 2017
0003-0894-91 sample1 BLISTER PACK in 1 CARTON (0003-0894-91) / 14 TABLET, FILM COATED in 1 BLISTER PACKDec 28, 2012

Recalls mentioning this NDC

Other Eliquis products