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Quetiapine Fumarate

NDC 16571-718 · Rising Pharma Holdings, Inc.

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

Packages

16571-718-01 — 100 TABLET, FILM COATED in 1 BOTTLE (16571-718-01)

16571-718-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (16571-718-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0904-6640 — Quetiapine, 0904-6641 — Quetiapine, 0904-6642 — Quetiapine, 0904-6643 — Quetiapine, 0904-6801 — Quetiapine, 0904-6802 — Quetiapine, 0904-6803 — Quetiapine, 0904-6804 — Quetiapine, 0904-6805 — Quetiapine, 16571-717 — Quetiapine Fumarate, 16571-719 — Quetiapine Fumarate, 16571-720 — Quetiapine Fumarate, 16571-721 — Quetiapine Fumarate, 16571-722 — Quetiapine Fumarate, 16571-809 — Quetiapine Fumarate, 16714-375 — Quetiapine Fumarate, 16714-376 — Quetiapine Fumarate, 16714-377 — Quetiapine Fumarate, 16714-378 — Quetiapine Fumarate, 16714-379 — Quetiapine Fumarate, +323 more

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