NDC 71335-1519 – Quetiapine Fumarate

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

Human Prescription Drug

Product NDC71335-1519

Product details

Brand name
Quetiapine Fumarate
Generic name
Quetiapine Fumarate
Labeler
Bryant Ranch Prepack
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 Fumarate →

Package NDC codes (5)

Package NDCDescriptionSince
71335-1519-130 TABLET, FILM COATED in 1 BOTTLE (71335-1519-1)Feb 20, 2020
71335-1519-2100 TABLET, FILM COATED in 1 BOTTLE (71335-1519-2)Apr 3, 2024
71335-1519-3120 TABLET, FILM COATED in 1 BOTTLE (71335-1519-3)Apr 3, 2024
71335-1519-490 TABLET, FILM COATED in 1 BOTTLE (71335-1519-4)Apr 3, 2024
71335-1519-560 TABLET, FILM COATED in 1 BOTTLE (71335-1519-5)Apr 3, 2024

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