Quetiapine

NDC 67046-1623 · Coupler LLC

Generic nameQuetiapine

Dosage formTABLET, EXTENDED RELEASE

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength200 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

67046-1623-3 — 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1623-3)

FDA lists these products with the same active ingredient.

65862-876 — Quetiapine, 65862-877 — Quetiapine, 67046-0487 — Quetiapine, 67046-0632 — quetiapine fumarate, 67046-0636 — quetiapine, 67046-0637 — quetiapine, 67046-0638 — quetiapine, 67046-1116 — quetiapine, 67046-1440 — Quetiapine fumarate, 67046-1588 — Quetiapine Fumarate, 67046-1649 — Quetiapine Fumarate, 67877-242 — Quetiapine, 67877-245 — Quetiapine, 67877-246 — Quetiapine, 67877-247 — Quetiapine, 67877-248 — Quetiapine, 67877-249 — Quetiapine, 67877-250 — Quetiapine, 68001-180 — quetiapine, 68001-181 — 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.