Quetiapine Fumarate

NDC 71335-9697 · Bryant Ranch Prepack

Generic nameQuetiapine Fumarate

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength300 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

71335-9697-1 — 30 TABLET, FILM COATED in 1 BOTTLE (71335-9697-1)

71335-9697-2 — 60 TABLET, FILM COATED in 1 BOTTLE (71335-9697-2)

71335-9697-3 — 28 TABLET, FILM COATED in 1 BOTTLE (71335-9697-3)

71335-9697-4 — 90 TABLET, FILM COATED in 1 BOTTLE (71335-9697-4)

FDA lists these products with the same active ingredient.

71335-2333 — Quetiapine Fumarate, 71335-2394 — Quetiapine Fumarate, 71335-2422 — quetiapine fumarate, 71335-2428 — quetiapine fumarate, 71335-2462 — quetiapine fumarate, 71335-2641 — Quetiapine, 71335-2679 — Quetiapine Fumarate, 71335-2691 — Quetiapine Fumarate, 71335-9623 — Quetiapine Fumarate, 71335-9627 — Quetiapine Fumarate, 71610-127 — Quetiapine Fumarate, 71610-128 — Quetiapine Fumarate, 71610-136 — Quetiapine Fumarate, 71610-140 — Quetiapine Fumarate, 71610-141 — Quetiapine Fumarate, 71610-702 — Quetiapine, 72189-340 — Quetiapine Fumarate, 72189-366 — Quetiapine Fumarate, 72189-446 — Quetiapine Fumarate, 72189-465 — 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.