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Quetiapine Fumarate

NDC 65862-873 · Aurobindo Pharma Limited

Generic nameQuetiapine
Dosage formTABLET, FILM COATED, EXTENDED RELEASE
RouteORAL
Active ingredient(s)QUETIAPINE FUMARATE
Strength50 mg/1
Pharmacologic classAtypical Antipsychotic [EPC]
Marketing categoryANDA

Packages

65862-873-01 — 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-873-01)

65862-873-05 — 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-873-05)

65862-873-60 — 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-873-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63629-4964 — QUETIAPINE FUMARATE, 63629-5944 — QUETIAPINE, 63629-7116 — Quetiapine, 65862-489 — Quetiapine Fumarate, 65862-490 — Quetiapine Fumarate, 65862-491 — Quetiapine Fumarate, 65862-492 — Quetiapine Fumarate, 65862-493 — Quetiapine Fumarate, 65862-494 — Quetiapine Fumarate, 65862-495 — Quetiapine Fumarate, 65862-874 — Quetiapine, 65862-875 — Quetiapine, 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, +323 more

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