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
- 63629-4964_a11c9785-4dd7-4064-a8b1-171c1677ed71
- Product NDC
- 63629-4964
- 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 — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (63629-4964-1) · 63629-4964-1
- 100 TABLET, FILM COATED in 1 BOTTLE (63629-4964-2) · 63629-4964-2
- 120 TABLET, FILM COATED in 1 BOTTLE (63629-4964-3) · 63629-4964-3
- 90 TABLET, FILM COATED in 1 BOTTLE (63629-4964-4) · 63629-4964-4
- 60 TABLET, FILM COATED in 1 BOTTLE (63629-4964-5) · 63629-4964-5
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 →