Quetiapine

NDC 71610-702 · Aphena Pharma Solutions - Tennessee, LLC

Generic nameQuetiapine

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength200 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

71610-702-15 — 15 TABLET, FILM COATED in 1 BOTTLE (71610-702-15)

71610-702-30 — 30 TABLET, FILM COATED in 1 BOTTLE (71610-702-30)

FDA lists these products with the same active ingredient.

71335-2679 — Quetiapine Fumarate, 71335-2691 — Quetiapine Fumarate, 71335-9623 — Quetiapine Fumarate, 71335-9627 — Quetiapine Fumarate, 71335-9697 — Quetiapine Fumarate, 71610-127 — Quetiapine Fumarate, 71610-128 — Quetiapine Fumarate, 71610-136 — Quetiapine Fumarate, 71610-140 — Quetiapine Fumarate, 71610-141 — Quetiapine Fumarate, 72189-340 — Quetiapine Fumarate, 72189-366 — Quetiapine Fumarate, 72189-446 — Quetiapine Fumarate, 72189-465 — Quetiapine Fumarate, 72189-477 — Quetiapine Fumarate, 72189-481 — Quetiapine Fumarate ER, 72189-482 — Quetiapine Fumarate ER, 72189-483 — Quetiapine Fumarate ER, 72189-519 — Quetiapine Fumarate ER, 72189-586 — Quetiapine Fumarate ER, +323 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.