Quetiapine Fumarate

NDC 50090-7471 · A-S Medication Solutions

Generic nameQuetiapine

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength200 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

50090-7471-0 — 30 TABLET, FILM COATED in 1 BOTTLE (50090-7471-0)

FDA lists these products with the same active ingredient.

47335-906 — Quetiapine fumarate, 47335-907 — Quetiapine fumarate, 50090-3333 — Quetiapine Fumarate, 50090-3342 — Quetiapine Fumarate, 50090-3377 — Quetiapine Fumarate, 50090-3983 — Quetiapine Fumarate, 50090-5473 — Quetiapine Fumarate, 50090-5884 — Quetiapine Fumarate, 50090-6337 — Quetiapine Fumarate, 50090-6812 — quetiapine fumarate, 50228-380 — Quetiapine, 50228-381 — Quetiapine, 50228-382 — Quetiapine, 50228-383 — Quetiapine, 50228-384 — Quetiapine, 50268-630 — Quetiapine Fumarate, 50268-631 — Quetiapine Fumarate, 50268-632 — Quetiapine Fumarate, 50268-633 — Quetiapine Fumarate, 50268-634 — 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.