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Aripiprazole

NDC 65162-901 · Amneal Pharmaceuticals LLC

Generic nameAripiprazole
Dosage formTABLET
RouteORAL
Active ingredient(s)ARIPIPRAZOLE
Strength20 mg/1
Pharmacologic classAtypical Antipsychotic [EPC]
Marketing categoryANDA

Packages

65162-901-03 — 30 TABLET in 1 BOTTLE (65162-901-03)

65162-901-09 — 90 TABLET in 1 BOTTLE (65162-901-09)

65162-901-11 — 1000 TABLET in 1 BOTTLE (65162-901-11)

65162-901-50 — 500 TABLET in 1 BOTTLE (65162-901-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62332-104 — Aripiprazole, 63187-965 — Aripiprazole, 63629-7003 — aripiprazole, 63629-7108 — aripiprazole, 63629-7774 — Aripiprazole, 65162-893 — Aripiprazole, 65162-896 — Aripiprazole, 65162-897 — Aripiprazole, 65162-898 — Aripiprazole, 65162-899 — Aripiprazole, 65162-902 — Aripiprazole, 65862-661 — 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, +246 more

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