Quetiapine

NDC 67877-248 · Ascend Laboratories, LLC

Generic nameQuetiapine

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength400 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

67877-248-01 — 100 TABLET, FILM COATED in 1 BOTTLE (67877-248-01)

67877-248-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (67877-248-10)

67877-248-33 — 1 BLISTER PACK in 1 CARTON (67877-248-33) / 10 TABLET, FILM COATED in 1 BLISTER PACK

67877-248-38 — 10 BLISTER PACK in 1 CARTON (67877-248-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

67046-0638 — quetiapine, 67046-1116 — quetiapine, 67046-1440 — Quetiapine fumarate, 67046-1588 — Quetiapine Fumarate, 67046-1623 — Quetiapine, 67046-1649 — Quetiapine Fumarate, 67877-242 — Quetiapine, 67877-245 — Quetiapine, 67877-246 — Quetiapine, 67877-247 — Quetiapine, 67877-249 — Quetiapine, 67877-250 — Quetiapine, 68001-180 — quetiapine, 68001-181 — quetiapine, 68001-182 — quetiapine, 68001-183 — quetiapine, 68001-184 — quetiapine, 68001-185 — quetiapine, 68001-598 — Quetiapine, 68001-599 — 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.