Quetiapine Fumarate

NDC 31722-767 · Camber Pharmaceuticals, Inc.

Generic nameQuetiapine Fumarate

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength200 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

31722-767-01 — 100 TABLET, FILM COATED in 1 BOTTLE (31722-767-01)

31722-767-05 — 500 TABLET, FILM COATED in 1 BOTTLE (31722-767-05)

31722-767-32 — 100 BLISTER PACK in 1 CARTON (31722-767-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-767-31)

31722-767-34 — 100 BLISTER PACK in 1 CARTON (31722-767-34) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-767-33)

FDA lists these products with the same active ingredient.

29300-151 — Quetiapine Fumarate, 29300-152 — Quetiapine Fumarate, 29300-308 — Quetiapine, 29300-309 — Quetiapine, 29300-310 — Quetiapine, 29300-311 — Quetiapine, 29300-312 — Quetiapine, 31722-764 — Quetiapine Fumarate, 31722-765 — Quetiapine Fumarate, 31722-766 — Quetiapine Fumarate, 31722-768 — Quetiapine Fumarate, 31722-769 — Quetiapine Fumarate, 33342-099 — Quetiapine fumarate, 33342-100 — Quetiapine fumarate, 33342-101 — Quetiapine fumarate, 33342-103 — Quetiapine fumarate, 33342-104 — Quetiapine fumarate, 33342-105 — Quetiapine fumarate, 33342-134 — QUETIAPINE, 33342-135 — 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.