NDC 71335-0772 – Quetiapine fumarate

Quetiapine Fumarate 300 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-0772

Product details

Brand name
Quetiapine fumarate
Generic name
Quetiapine fumarate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA201190
Marketed since
March 28, 2012
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Quetiapine Fumarate →

Package NDC codes (4)

Package NDCDescriptionSince
71335-0772-130 TABLET, FILM COATED in 1 BOTTLE (71335-0772-1)Apr 11, 2018
71335-0772-260 TABLET, FILM COATED in 1 BOTTLE (71335-0772-2)May 2, 2022
71335-0772-328 TABLET, FILM COATED in 1 BOTTLE (71335-0772-3)May 2, 2022
71335-0772-490 TABLET, FILM COATED in 1 BOTTLE (71335-0772-4)May 2, 2022

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