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
- 63629-4841_8042cb5a-fa9c-4089-98dc-00d012cb7ccd
- Product NDC
- 63629-4841
- Form
- TABLET, FILM COATED
- Composition / generic term
- QUETIAPINE FUMARATE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120328
- Source listing expiry
- 20271231
Source-listed ingredients
- QUETIAPINE FUMARATE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (63629-4841-1) · 63629-4841-1
- 60 TABLET, FILM COATED in 1 BOTTLE (63629-4841-2) · 63629-4841-2
- 90 TABLET, FILM COATED in 1 BOTTLE (63629-4841-3) · 63629-4841-3
- 25 TABLET, FILM COATED in 1 BOTTLE (63629-4841-4) · 63629-4841-4
- 120 TABLET, FILM COATED in 1 BOTTLE (63629-4841-5) · 63629-4841-5
Source and coverage
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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.
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