NDC 71610-769 – Sertraline

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

Human Prescription Drug

Product NDC71610-769

Product details

Brand name
Sertraline
Generic name
Sertraline
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077397
Marketed since
August 20, 2012
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sertraline →

Package NDC codes (7)

Package NDCDescriptionSince
71610-769-1515 TABLET, FILM COATED in 1 BOTTLE (71610-769-15)Jan 17, 2024
71610-769-3030 TABLET, FILM COATED in 1 BOTTLE (71610-769-30)Mar 7, 2024
71610-769-4545 TABLET, FILM COATED in 1 BOTTLE (71610-769-45)Jan 17, 2024
71610-769-5360 TABLET, FILM COATED in 1 BOTTLE (71610-769-53)Jan 17, 2024
71610-769-6090 TABLET, FILM COATED in 1 BOTTLE (71610-769-60)Jan 17, 2024
71610-769-73135 TABLET, FILM COATED in 1 BOTTLE (71610-769-73)Jan 17, 2024
71610-769-80180 TABLET, FILM COATED in 1 BOTTLE (71610-769-80)Jan 17, 2024

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