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Aripiprazole

NDC 72865-158 · XLCare Pharmaceuticals, Inc.

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

Packages

72865-158-05 — 500 TABLET in 1 BOTTLE (72865-158-05)

72865-158-30 — 30 TABLET in 1 BOTTLE (72865-158-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72189-476 — Aripiprazole, 72578-106 — Aripiprazole, 72578-107 — Aripiprazole, 72603-445 — Aripiprazole oral, 72789-462 — Aripiprazole, 72865-153 — Aripiprazole, 72865-154 — Aripiprazole, 72865-155 — Aripiprazole, 72865-156 — Aripiprazole, 72865-157 — Aripiprazole, 72865-180 — Aripiprazole, 72865-181 — Aripiprazole, 72865-182 — Aripiprazole, 72865-183 — Aripiprazole, 72865-184 — Aripiprazole, 72865-185 — Aripiprazole, 72888-100 — Aripiprazole, 76282-044 — Aripiprazole, 76282-045 — Aripiprazole, 76282-046 — 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.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels