NDC 76420-518 – Quetiapine

Quetiapine Fumarate 200 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC76420-518

Product details

Brand name
Quetiapine
Generic name
Quetiapine
Labeler
ASCLEMED USA INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA201504
Marketed since
March 1, 2013
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Quetiapine →

Package NDC codes (6)

Package NDCDescriptionSince
76420-518-01100 TABLET, FILM COATED in 1 BOTTLE (76420-518-01)Oct 21, 2025
76420-518-1010 TABLET, FILM COATED in 1 BOTTLE (76420-518-10)Oct 21, 2025
76420-518-2020 TABLET, FILM COATED in 1 BOTTLE (76420-518-20)Oct 21, 2025
76420-518-3030 TABLET, FILM COATED in 1 BOTTLE (76420-518-30)Oct 21, 2025
76420-518-6060 TABLET, FILM COATED in 1 BOTTLE (76420-518-60)Oct 21, 2025
76420-518-9090 TABLET, FILM COATED in 1 BOTTLE (76420-518-90)Oct 21, 2025

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