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Aripiprazole

NDC 46708-259 · Alembic Pharmaceuticals Limited

Generic nameAripiprazole
Dosage formTABLET
RouteORAL
Active ingredient(s)ARIPIPRAZOLE
Strength30 mg/1
Pharmacologic classAtypical Antipsychotic [EPC]
Marketing categoryANDA

Packages

46708-259-10 — 100 TABLET in 1 CARTON (46708-259-10)

46708-259-30 — 30 TABLET in 1 BOTTLE (46708-259-30)

46708-259-31 — 100 TABLET in 1 BOTTLE (46708-259-31)

46708-259-71 — 500 TABLET in 1 BOTTLE (46708-259-71)

46708-259-91 — 1000 TABLET in 1 BOTTLE (46708-259-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43598-966 — Aripiprazole, 43598-967 — Aripiprazole, 43598-968 — Aripiprazole, 43598-969 — Aripiprazole, 43598-970 — Aripiprazole, 46708-254 — Aripiprazole, 46708-255 — Aripiprazole, 46708-256 — Aripiprazole, 46708-257 — Aripiprazole, 46708-258 — Aripiprazole, 46708-260 — Aripiprazole, 46708-261 — Aripiprazole, 50090-4665 — Aripiprazole, 50090-4863 — Aripiprazole, 50090-4936 — Aripiprazole, 50090-6063 — ARIPIPRAZOLE, 50090-6403 — Aripiprazole, 50090-6409 — Aripiprazole, 50090-6563 — aripiprazole, 50090-7105 — aripiprazole, +246 more

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