Quetiapine fumarate

NDC 71335-2176 · Bryant Ranch Prepack

Generic nameQuetiapine fumarate

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength50 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

71335-2176-1 — 30 TABLET, FILM COATED in 1 BOTTLE (71335-2176-1)

71335-2176-2 — 60 TABLET, FILM COATED in 1 BOTTLE (71335-2176-2)

71335-2176-3 — 90 TABLET, FILM COATED in 1 BOTTLE (71335-2176-3)

71335-2176-4 — 25 TABLET, FILM COATED in 1 BOTTLE (71335-2176-4)

71335-2176-5 — 120 TABLET, FILM COATED in 1 BOTTLE (71335-2176-5)

FDA lists these products with the same active ingredient.

71205-826 — Quetiapine Fumarate, 71335-0772 — Quetiapine fumarate, 71335-0926 — Quetiapine Fumarate, 71335-1353 — Quetiapine Fumarate, 71335-1362 — Quetiapine fumarate, 71335-1462 — Quetiapine, 71335-1519 — Quetiapine Fumarate, 71335-1562 — Quetiapine Fumarate, 71335-1709 — Quetiapine Fumarate, 71335-2157 — 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, 71335-2641 — Quetiapine, 71335-2679 — Quetiapine Fumarate, 71335-2691 — Quetiapine Fumarate, 71335-9623 — 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.