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Aripiprazole

NDC 67877-435 · Ascend Laboratories, LLC

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

Packages

67877-435-01 — 100 TABLET in 1 BOTTLE (67877-435-01)

67877-435-03 — 30 TABLET in 1 BOTTLE (67877-435-03)

67877-435-05 — 500 TABLET in 1 BOTTLE (67877-435-05)

67877-435-38 — 10 BLISTER PACK in 1 CARTON (67877-435-38) / 10 TABLET in 1 BLISTER PACK (67877-435-33)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67046-1017 — Aripiprazole, 67046-1052 — Aripiprazole, 67046-1085 — Aripiprazole, 67046-1638 — Aripiprazole, 67046-2046 — Aripiprazole, 67877-430 — Aripiprazole, 67877-431 — Aripiprazole, 67877-432 — Aripiprazole, 67877-433 — Aripiprazole, 67877-434 — Aripiprazole, 68071-3725 — Aripiprazole, 68071-3848 — Aripiprazole, 68071-3850 — Aripiprazole, 68071-3906 — Aripiprazole, 68788-7063 — aripiprazole, 68788-7733 — Aripiprazole, 68788-7749 — Aripiprazole, 68788-7808 — Aripiprazole, 68788-8089 — Aripiprazole, 68788-8502 — 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.