Quetiapine

NDC 72789-266 · PD-Rx Pharmaceuticals, Inc.

Generic nameQuetiapine

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength50 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

72789-266-07 — 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-266-07)

FDA lists these products with the same active ingredient.

72189-366 — Quetiapine Fumarate, 72189-446 — Quetiapine Fumarate, 72189-465 — Quetiapine Fumarate, 72189-477 — Quetiapine Fumarate, 72189-481 — Quetiapine Fumarate ER, 72189-482 — Quetiapine Fumarate ER, 72189-483 — Quetiapine Fumarate ER, 72189-519 — Quetiapine Fumarate ER, 72189-586 — Quetiapine Fumarate ER, 72189-642 — Quetiapine Fumarate ER, 72865-264 — Quetiapine Fumarate, 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, +323 more

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