NDC 71335-1362 – Quetiapine fumarate

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

Human Prescription Drug

Product NDC71335-1362

Product details

Brand name
Quetiapine fumarate
Generic name
Quetiapine fumarate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203359
Marketed since
June 14, 2016
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
71335-1362-130 TABLET, FILM COATED in 1 BOTTLE (71335-1362-1)Oct 3, 2019
71335-1362-2100 TABLET, FILM COATED in 1 BOTTLE (71335-1362-2)May 20, 2024
71335-1362-3120 TABLET, FILM COATED in 1 BOTTLE (71335-1362-3)May 20, 2024
71335-1362-490 TABLET, FILM COATED in 1 BOTTLE (71335-1362-4)May 20, 2024
71335-1362-560 TABLET, FILM COATED in 1 BOTTLE (71335-1362-5)May 20, 2024

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