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
29300-151_9054a1a7-c7ea-4630-be0b-2dcbe910ca94
Product NDC
29300-151
Form
TABLET, FILM COATED
Composition / generic term
Quetiapine Fumarate
Labeler
Unichem Pharmaceuticals (USA), Inc.
Marketing category
ANDA
Marketing start / end (source format)
20160701
Source listing expiry
20261231

Source-listed ingredients

  • QUETIAPINE FUMARATE — 300 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-151-01) · 29300-151-01
  • 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-151-10) · 29300-151-10
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-151-16) · 29300-151-16

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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