Aripiprazole

NDC 65862-666 · Aurobindo Pharma Limited

Generic nameAripiprazole

Dosage formTABLET

RouteORAL

Active ingredient(s)ARIPIPRAZOLE

Strength30 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

65862-666-01 — 100 TABLET in 1 BOTTLE (65862-666-01)

65862-666-05 — 500 TABLET in 1 BOTTLE (65862-666-05)

65862-666-30 — 30 TABLET in 1 BOTTLE (65862-666-30)

65862-666-78 — 10 BLISTER PACK in 1 CARTON (65862-666-78) / 10 TABLET in 1 BLISTER PACK (65862-666-10)

FDA lists these products with the same active ingredient.

65162-897 — Aripiprazole, 65162-898 — Aripiprazole, 65162-899 — Aripiprazole, 65162-901 — Aripiprazole, 65162-902 — Aripiprazole, 65862-661 — Aripiprazole, 65862-662 — Aripiprazole, 65862-663 — Aripiprazole, 65862-664 — Aripiprazole, 65862-665 — Aripiprazole, 66689-735 — Aripiprazole, 67046-0492 — Aripiprazole, 67046-0873 — Aripiprazole, 67046-0885 — Aripiprazole, 67046-1017 — Aripiprazole, 67046-1052 — Aripiprazole, 67046-1085 — Aripiprazole, 67046-1638 — Aripiprazole, 67046-2046 — Aripiprazole, 67877-430 — 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.