Quetiapine

NDC 71093-139 · ACI Healthcare USA, Inc.

Generic nameQuetiapine

Dosage formTABLET, FILM COATED, EXTENDED RELEASE

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength400 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

71093-139-02 — 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71093-139-02)

FDA lists these products with the same active ingredient.

70518-4437 — Quetiapine, 70518-4451 — Quetiapine, 70518-4699 — QUETIAPINE, 70518-4700 — QUETIAPINE, 70518-4701 — Quetiapine Fumarate, 70518-4705 — Quetiapine Fumarate, 71093-135 — Quetiapine, 71093-136 — Quetiapine, 71093-137 — Quetiapine, 71093-138 — Quetiapine, 71205-026 — Quetiapine, 71205-031 — Quetiapine Fumarate, 71205-401 — Quetiapine, 71205-402 — Quetiapine, 71205-788 — Quetiapine Fumarate, 71205-826 — Quetiapine Fumarate, 71335-0772 — Quetiapine fumarate, 71335-0926 — Quetiapine Fumarate, 71335-1353 — Quetiapine Fumarate, 71335-1362 — Quetiapine fumarate, +323 more

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