NDC 71335-1078 – Sertraline Hydrochloride

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

Human Prescription Drug

Product NDC71335-1078

Product details

Brand name
Sertraline Hydrochloride
Generic name
Sertraline Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202825
Marketed since
February 9, 2017
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sertraline hydrochloride →

Package NDC codes (7)

Package NDCDescriptionSince
71335-1078-130 TABLET, FILM COATED in 1 BOTTLE (71335-1078-1)Jan 29, 2019
71335-1078-260 TABLET, FILM COATED in 1 BOTTLE (71335-1078-2)Feb 14, 2019
71335-1078-390 TABLET, FILM COATED in 1 BOTTLE (71335-1078-3)Feb 5, 2019
71335-1078-4180 TABLET, FILM COATED in 1 BOTTLE (71335-1078-4)Apr 2, 2024
71335-1078-528 TABLET, FILM COATED in 1 BOTTLE (71335-1078-5)Apr 2, 2024
71335-1078-6120 TABLET, FILM COATED in 1 BOTTLE (71335-1078-6)Apr 2, 2024
71335-1078-7100 TABLET, FILM COATED in 1 BOTTLE (71335-1078-7)Jun 4, 2026

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