Aripiprazole

NDC 65862-661 · Aurobindo Pharma Limited

Generic nameAripiprazole

Dosage formTABLET

RouteORAL

Active ingredient(s)ARIPIPRAZOLE

Strength2 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

65862-661-01 — 100 TABLET in 1 BOTTLE (65862-661-01)

65862-661-05 — 500 TABLET in 1 BOTTLE (65862-661-05)

65862-661-30 — 30 TABLET in 1 BOTTLE (65862-661-30)

65862-661-78 — 10 BLISTER PACK in 1 CARTON (65862-661-78) / 10 TABLET in 1 BLISTER PACK (65862-661-10)

FDA lists these products with the same active ingredient.

63629-7003 — aripiprazole, 63629-7108 — aripiprazole, 63629-7774 — Aripiprazole, 65162-893 — Aripiprazole, 65162-896 — Aripiprazole, 65162-897 — Aripiprazole, 65162-898 — Aripiprazole, 65162-899 — Aripiprazole, 65162-901 — Aripiprazole, 65162-902 — Aripiprazole, 65862-662 — Aripiprazole, 65862-663 — Aripiprazole, 65862-664 — Aripiprazole, 65862-665 — Aripiprazole, 65862-666 — Aripiprazole, 66689-735 — Aripiprazole, 67046-0492 — Aripiprazole, 67046-0873 — Aripiprazole, 67046-0885 — Aripiprazole, 67046-1017 — Aripiprazole, +246 more

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