United States · FDA National Drug Code directory

Quetiapine Extended Release

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
70518-4051_5412bcbf-8105-19db-e063-6294a90a5fd7
Product NDC
70518-4051
Form
TABLET, FILM COATED, EXTENDED RELEASE
Composition / generic term
Quetiapine
Labeler
REMEDYREPACK INC.
Marketing category
ANDA
Marketing start / end (source format)
20240413
Source listing expiry
20271231

Source-listed ingredients

  • QUETIAPINE FUMARATE — 150 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4051-0) · 70518-4051-0

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 →