Quetiapine

NDC 29300-310 · Unichem Pharmaceuticals (USA), Inc.

Generic nameQuetiapine

Dosage formTABLET, EXTENDED RELEASE

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength200 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

29300-310-16 — 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (29300-310-16)

FDA lists these products with the same active ingredient.

16729-149 — Quetiapine, 16729-150 — Quetiapine, 29300-147 — Quetiapine Fumarate, 29300-148 — Quetiapine Fumarate, 29300-149 — Quetiapine Fumarate, 29300-150 — Quetiapine Fumarate, 29300-151 — Quetiapine Fumarate, 29300-152 — Quetiapine Fumarate, 29300-308 — Quetiapine, 29300-309 — Quetiapine, 29300-311 — Quetiapine, 29300-312 — Quetiapine, 31722-764 — Quetiapine Fumarate, 31722-765 — Quetiapine Fumarate, 31722-766 — Quetiapine Fumarate, 31722-767 — Quetiapine Fumarate, 31722-768 — Quetiapine Fumarate, 31722-769 — Quetiapine Fumarate, 33342-099 — Quetiapine fumarate, 33342-100 — 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.