Apixaban

NDC 0115-1722 · Amneal Pharmaceuticals of New York LLC

Generic nameApixaban

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)APIXABAN

Strength5 mg/1

Pharmacologic classFactor Xa Inhibitor [EPC], Factor Xa Inhibitors [MoA]

Marketing categoryANDA

Packages

0115-1722-01 — 10 BLISTER PACK in 1 CARTON (0115-1722-01) / 10 TABLET, FILM COATED in 1 BLISTER PACK (0115-1722-15)

0115-1722-03 — 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0115-1722-03)

0115-1722-13 — 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0115-1722-13)

FDA lists these products with the same active ingredient.

0003-0893 — apixaban, 0003-0894 — apixaban, 0003-0898 — apixaban, 0003-1028 — apixaban, 0115-1721 — Apixaban, 14445-149 — apixaban, 14445-150 — apixaban, 33342-337 — Apixaban, 33342-338 — Apixaban, 50090-1436 — apixaban, 50090-1437 — apixaban, 50090-6451 — apixaban, 50090-6454 — apixaban, 55154-0612 — apixaban, 55154-0613 — apixaban, 70518-4462 — apixaban, 71610-662 — apixaban, 71610-811 — apixaban, 82804-085 — apixaban

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.