Quetiapine Fumarate

NDC 50742-638 · Ingenus Pharmaceuticals, LLC

Generic namequetiapine fumarate

Dosage formTABLET, EXTENDED RELEASE

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength300 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

50742-638-10 — 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-638-10)

50742-638-30 — 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-638-30)

50742-638-60 — 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-638-60)

50742-638-90 — 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-638-90)

FDA lists these products with the same active ingredient.

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, 50742-636 — quetiapine fumarate, 50742-637 — quetiapine fumarate, 50742-639 — quetiapine fumarate, 51407-066 — Quetiapine Fumarate, 51407-067 — Quetiapine Fumarate, 51407-068 — Quetiapine Fumarate, 51407-069 — Quetiapine Fumarate, 51407-070 — Quetiapine Fumarate, 51407-071 — Quetiapine Fumarate, 51407-799 — Quetiapine, 51407-800 — Quetiapine, 51407-801 — 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.