Quetiapine

NDC 71335-2641 · Bryant Ranch Prepack

Generic nameQuetiapine

Dosage formTABLET, EXTENDED RELEASE

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength400 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

71335-2641-1 — 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2641-1)

FDA lists these products with the same active ingredient.

71335-1562 — Quetiapine Fumarate, 71335-1709 — Quetiapine Fumarate, 71335-2157 — Quetiapine fumarate, 71335-2176 — Quetiapine fumarate, 71335-2278 — quetiapine fumarate, 71335-2333 — Quetiapine Fumarate, 71335-2394 — Quetiapine Fumarate, 71335-2422 — quetiapine fumarate, 71335-2428 — quetiapine fumarate, 71335-2462 — quetiapine fumarate, 71335-2679 — Quetiapine Fumarate, 71335-2691 — Quetiapine Fumarate, 71335-9623 — Quetiapine Fumarate, 71335-9627 — Quetiapine Fumarate, 71335-9697 — Quetiapine Fumarate, 71610-127 — Quetiapine Fumarate, 71610-128 — Quetiapine Fumarate, 71610-136 — Quetiapine Fumarate, 71610-140 — Quetiapine Fumarate, 71610-141 — 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.