Quetiapine

NDC 0904-6802 · Major Pharmaceuticals

Generic nameQuetiapine

Dosage formTABLET, FILM COATED, EXTENDED RELEASE

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength150 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

0904-6802-61 — 100 BLISTER PACK in 1 CARTON (0904-6802-61) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

0615-8473 — Quetiapine Fumarate, 0615-8474 — Quetiapine Fumarate, 0615-8568 — Quetiapine Fumarate, 0904-6638 — Quetiapine, 0904-6639 — Quetiapine, 0904-6640 — Quetiapine, 0904-6641 — Quetiapine, 0904-6642 — Quetiapine, 0904-6643 — Quetiapine, 0904-6801 — Quetiapine, 0904-6803 — Quetiapine, 0904-6804 — Quetiapine, 0904-6805 — Quetiapine, 16571-717 — Quetiapine Fumarate, 16571-718 — Quetiapine Fumarate, 16571-719 — Quetiapine Fumarate, 16571-720 — Quetiapine Fumarate, 16571-721 — Quetiapine Fumarate, 16571-722 — Quetiapine Fumarate, 16571-809 — 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.