Quetiapine

NDC 76420-519 · ASCLEMED USA INC.

Generic nameQuetiapine

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength300 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

76420-519-01 — 10 BLISTER PACK in 1 CARTON (76420-519-01) / 10 TABLET, FILM COATED in 1 BLISTER PACK

76420-519-10 — 10 TABLET, FILM COATED in 1 BOTTLE (76420-519-10)

76420-519-20 — 20 TABLET, FILM COATED in 1 BOTTLE (76420-519-20)

76420-519-30 — 30 TABLET, FILM COATED in 1 BOTTLE (76420-519-30)

76420-519-60 — 60 TABLET, FILM COATED in 1 BOTTLE (76420-519-60)

76420-519-90 — 90 TABLET, FILM COATED in 1 BOTTLE (76420-519-90)

FDA lists these products with the same active ingredient.

72865-265 — Quetiapine Fumarate, 72865-266 — Quetiapine Fumarate, 72865-267 — Quetiapine Fumarate, 72865-268 — Quetiapine Fumarate, 72865-269 — Quetiapine Fumarate, 76420-512 — Quetiapine, 76420-513 — Quetiapine, 76420-514 — Quetiapine, 76420-516 — Quetiapine, 76420-518 — Quetiapine, 76420-522 — Quetiapine, 80425-0184 — Quetiapine Fumarate, 80425-0186 — Quetiapine Fumarate, 80425-0413 — quetiapine fumarate, 82009-095 — quetiapine fumarate, 82009-096 — quetiapine fumarate, 82009-097 — quetiapine fumarate, 82009-098 — quetiapine fumarate, 82804-020 — Quetiapine Fumarate, 82804-094 — 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.