NDC 71335-0808 – Sertraline Hydrochloride

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

Human Prescription Drug

Product NDC71335-0808

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 (6)

Package NDCDescriptionSince
71335-0808-130 TABLET, FILM COATED in 1 BOTTLE (71335-0808-1)Jun 25, 2018
71335-0808-260 TABLET, FILM COATED in 1 BOTTLE (71335-0808-2)May 3, 2018
71335-0808-390 TABLET, FILM COATED in 1 BOTTLE (71335-0808-3)May 16, 2018
71335-0808-4180 TABLET, FILM COATED in 1 BOTTLE (71335-0808-4)May 22, 2024
71335-0808-528 TABLET, FILM COATED in 1 BOTTLE (71335-0808-5)May 22, 2024
71335-0808-6120 TABLET, FILM COATED in 1 BOTTLE (71335-0808-6)Nov 8, 2023

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