Quetiapine

NDC 50228-381 · ScieGen Pharmaceuticals, Inc

Generic nameQuetiapine

Dosage formTABLET, FILM COATED, EXTENDED RELEASE

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength150 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

50228-381-10 — 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50228-381-10)

50228-381-30 — 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50228-381-30)

50228-381-60 — 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50228-381-60)

FDA lists these products with the same active ingredient.

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, 50090-7471 — Quetiapine, 50228-380 — 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, 50268-635 — Quetiapine Fumarate, 50742-635 — 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.