NDC 71335-2659 – Sertraline

Sertraline Hydrochloride 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2659

Product details

Brand name
Sertraline
Generic name
Sertraline
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076465
Marketed since
February 23, 2023
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sertraline →

Package NDC codes (7)

Package NDCDescriptionSince
71335-2659-130 TABLET, FILM COATED in 1 BOTTLE (71335-2659-1)Jun 23, 2025
71335-2659-260 TABLET, FILM COATED in 1 BOTTLE (71335-2659-2)Jun 23, 2025
71335-2659-390 TABLET, FILM COATED in 1 BOTTLE (71335-2659-3)Jun 23, 2025
71335-2659-4180 TABLET, FILM COATED in 1 BOTTLE (71335-2659-4)Jun 23, 2025
71335-2659-528 TABLET, FILM COATED in 1 BOTTLE (71335-2659-5)Jun 23, 2025
71335-2659-6120 TABLET, FILM COATED in 1 BOTTLE (71335-2659-6)Jun 23, 2025
71335-2659-7100 TABLET, FILM COATED in 1 BOTTLE (71335-2659-7)Jun 23, 2025

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