NDC 71335-0210 – Sertraline Hydrochloride

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

Human Prescription Drug

Product NDC71335-0210

Product details

Brand name
Sertraline Hydrochloride
Generic name
Sertraline Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077206
Marketed since
February 6, 2007
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

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

Package NDC codes (9)

Package NDCDescriptionSince
71335-0210-130 TABLET, FILM COATED in 1 BOTTLE (71335-0210-1)Jun 12, 2019
71335-0210-260 TABLET, FILM COATED in 1 BOTTLE (71335-0210-2)Jun 11, 2019
71335-0210-390 TABLET, FILM COATED in 1 BOTTLE (71335-0210-3)May 21, 2019
71335-0210-4180 TABLET, FILM COATED in 1 BOTTLE (71335-0210-4)Sep 26, 2019
71335-0210-528 TABLET, FILM COATED in 1 BOTTLE (71335-0210-5)Dec 27, 2021
71335-0210-615 TABLET, FILM COATED in 1 BOTTLE (71335-0210-6)Dec 27, 2021
71335-0210-7120 TABLET, FILM COATED in 1 BOTTLE (71335-0210-7)Dec 27, 2021
71335-0210-8100 TABLET, FILM COATED in 1 BOTTLE (71335-0210-8)Dec 27, 2021
71335-0210-945 TABLET, FILM COATED in 1 BOTTLE (71335-0210-9)Dec 27, 2021

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