NDC 71335-0510 – Sertraline Hydrochloride

Sertraline Hydrochloride 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-0510

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 (9)

Package NDCDescriptionSince
71335-0510-130 TABLET, FILM COATED in 1 BOTTLE (71335-0510-1)Mar 23, 2018
71335-0510-260 TABLET, FILM COATED in 1 BOTTLE (71335-0510-2)Mar 21, 2018
71335-0510-390 TABLET, FILM COATED in 1 BOTTLE (71335-0510-3)Apr 9, 2018
71335-0510-4180 TABLET, FILM COATED in 1 BOTTLE (71335-0510-4)Feb 12, 2018
71335-0510-528 TABLET, FILM COATED in 1 BOTTLE (71335-0510-5)Apr 3, 2024
71335-0510-615 TABLET, FILM COATED in 1 BOTTLE (71335-0510-6)Apr 3, 2024
71335-0510-7120 TABLET, FILM COATED in 1 BOTTLE (71335-0510-7)Apr 3, 2024
71335-0510-8100 TABLET, FILM COATED in 1 BOTTLE (71335-0510-8)Apr 3, 2024
71335-0510-945 TABLET, FILM COATED in 1 BOTTLE (71335-0510-9)Aug 31, 2022

Other Sertraline hydrochloride products