Quetiapine fumarate

NDC 47335-906 · Sun Pharmaceutical Industries, Inc.

Generic nameQuetiapine fumarate

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength300 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

47335-906-61 — 10 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-906-61) / 10 TABLET, FILM COATED in 1 BLISTER PACK

47335-906-83 — 30 TABLET, FILM COATED in 1 BOTTLE (47335-906-83)

47335-906-86 — 60 TABLET, FILM COATED in 1 BOTTLE (47335-906-86)

FDA lists these products with the same active ingredient.

46708-134 — quetiapine fumarate, 46708-135 — quetiapine fumarate, 46708-136 — quetiapine fumarate, 46708-137 — quetiapine fumarate, 46708-138 — quetiapine fumarate, 46708-139 — quetiapine fumarate, 47335-902 — Quetiapine fumarate, 47335-903 — Quetiapine fumarate, 47335-904 — Quetiapine fumarate, 47335-905 — Quetiapine fumarate, 47335-907 — Quetiapine fumarate, 50090-3333 — Quetiapine Fumarate, 50090-3342 — Quetiapine Fumarate, 50090-3377 — Quetiapine Fumarate, 50090-3983 — Quetiapine Fumarate, 50090-5473 — Quetiapine Fumarate, 50090-5884 — Quetiapine Fumarate, 50090-6337 — Quetiapine Fumarate, 50090-6812 — quetiapine fumarate, 50090-7471 — 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.