Quetiapine Fumarate

NDC 71335-1519 · Bryant Ranch Prepack

Generic nameQuetiapine Fumarate

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength200 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

71335-1519-1 — 30 TABLET, FILM COATED in 1 BOTTLE (71335-1519-1)

71335-1519-2 — 100 TABLET, FILM COATED in 1 BOTTLE (71335-1519-2)

71335-1519-3 — 120 TABLET, FILM COATED in 1 BOTTLE (71335-1519-3)

71335-1519-4 — 90 TABLET, FILM COATED in 1 BOTTLE (71335-1519-4)

71335-1519-5 — 60 TABLET, FILM COATED in 1 BOTTLE (71335-1519-5)

FDA lists these products with the same active ingredient.

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, 71335-1462 — Quetiapine, 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, +323 more

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