Quetiapine Fumarate

NDC 68788-8859 · Preferred Pharmaceuticals Inc.

Generic nameQuetiapine Fumarate

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength200 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

68788-8859-1 — 100 TABLET, FILM COATED in 1 BOTTLE (68788-8859-1)

68788-8859-3 — 30 TABLET, FILM COATED in 1 BOTTLE (68788-8859-3)

68788-8859-6 — 60 TABLET, FILM COATED in 1 BOTTLE (68788-8859-6)

68788-8859-8 — 120 TABLET, FILM COATED in 1 BOTTLE (68788-8859-8)

68788-8859-9 — 90 TABLET, FILM COATED in 1 BOTTLE (68788-8859-9)

FDA lists these products with the same active ingredient.

68180-614 — Quetiapine, 68180-615 — Quetiapine, 68180-616 — Quetiapine, 68788-7813 — Quetiapine Fumarate, 68788-8530 — Quetiapine Fumarate, 68788-8745 — quetiapine fumarate, 68788-8746 — quetiapine fumarate, 68788-8764 — quetiapine fumarate, 68788-8778 — quetiapine fumarate, 68788-8823 — Quetiapine Fumarate, 69948-002 — Quetiapine, 69948-003 — Quetiapine, 70518-1918 — quetiapine fumarate, 70518-1919 — quetiapine fumarate, 70518-2102 — quetiapine fumarate, 70518-2175 — Quetiapine Fumarate, 70518-2752 — quetiapine fumarate, 70518-2901 — quetiapine fumarate, 70518-3429 — Quetiapine Fumarate, 70518-3581 — 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.