NDC 65862-012 – Sertraline Hydrochloride

Sertraline Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC65862-012

Product details

Brand name
Sertraline Hydrochloride
Generic name
Sertraline Hydrochloride
Labeler
Aurobindo Pharma Limited
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 (8)

Package NDCDescriptionSince
65862-012-01100 TABLET, FILM COATED in 1 BOTTLE (65862-012-01)Feb 6, 2007
65862-012-05500 TABLET, FILM COATED in 1 BOTTLE (65862-012-05)Feb 6, 2007
65862-012-3030 TABLET, FILM COATED in 1 BOTTLE (65862-012-30)Feb 6, 2007
65862-012-5050 TABLET, FILM COATED in 1 BOTTLE (65862-012-50)Feb 6, 2007
65862-012-515000 TABLET, FILM COATED in 1 BOTTLE (65862-012-51)Feb 6, 2007
65862-012-6060 TABLET, FILM COATED in 1 BOTTLE (65862-012-60)Feb 6, 2007
65862-012-9090 TABLET, FILM COATED in 1 BOTTLE (65862-012-90)Feb 6, 2007
65862-012-991000 TABLET, FILM COATED in 1 BOTTLE (65862-012-99)Feb 6, 2007

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