United States · FDA National Drug Code directory
Quetiapine fumarate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 33342-105_e8676630-c511-427b-af62-969f338d96cf
- Product NDC
- 33342-105
- Form
- TABLET, FILM COATED
- Composition / generic term
- Quetiapine fumarate
- Labeler
- Macleods Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160614
- Source listing expiry
- 20261231
Source-listed ingredients
- QUETIAPINE FUMARATE — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (33342-105-11) · 33342-105-11
- 500 TABLET, FILM COATED in 1 BOTTLE (33342-105-15) · 33342-105-15
- 9 BLISTER PACK in 1 CARTON (33342-105-39) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 33342-105-39
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →