Quetiapine Fumarate

NDC 16714-379 · NorthStar Rx LLC

Generic nameQuetiapine Fumarate

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength300 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

16714-379-01 — 100 TABLET, FILM COATED in 1 BOTTLE (16714-379-01)

FDA lists these products with the same active ingredient.

16571-718 — Quetiapine Fumarate, 16571-719 — Quetiapine Fumarate, 16571-720 — Quetiapine Fumarate, 16571-721 — Quetiapine Fumarate, 16571-722 — Quetiapine Fumarate, 16571-809 — Quetiapine Fumarate, 16714-375 — Quetiapine Fumarate, 16714-376 — Quetiapine Fumarate, 16714-377 — Quetiapine Fumarate, 16714-378 — Quetiapine Fumarate, 16714-380 — Quetiapine Fumarate, 16729-095 — QUETIAPINE FUMARATE, 16729-096 — QUETIAPINE FUMARATE, 16729-097 — QUETIAPINE FUMARATE, 16729-109 — QUETIAPINE FUMARATE, 16729-132 — QUETIAPINE FUMARATE, 16729-145 — Quetiapine, 16729-146 — Quetiapine, 16729-147 — Quetiapine, 16729-148 — 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.