NDC 71335-0322 – Escitalopram oxalate

Escitalopram Oxalate 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-0322

Product details

Brand name
Escitalopram oxalate
Generic name
Escitalopram oxalate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090939
Marketed since
September 11, 2012
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Escitalopram oxalate →

Package NDC codes (9)

Package NDCDescriptionSince
71335-0322-130 TABLET, FILM COATED in 1 BOTTLE (71335-0322-1)Sep 21, 2023
71335-0322-228 TABLET, FILM COATED in 1 BOTTLE (71335-0322-2)Oct 30, 2024
71335-0322-360 TABLET, FILM COATED in 1 BOTTLE (71335-0322-3)Aug 22, 2023
71335-0322-490 TABLET, FILM COATED in 1 BOTTLE (71335-0322-4)Aug 17, 2023
71335-0322-510 TABLET, FILM COATED in 1 BOTTLE (71335-0322-5)Oct 30, 2024
71335-0322-6120 TABLET, FILM COATED in 1 BOTTLE (71335-0322-6)Oct 30, 2024
71335-0322-77 TABLET, FILM COATED in 1 BOTTLE (71335-0322-7)Oct 30, 2024
71335-0322-8180 TABLET, FILM COATED in 1 BOTTLE (71335-0322-8)Oct 30, 2024
71335-0322-9100 TABLET, FILM COATED in 1 BOTTLE (71335-0322-9)Oct 30, 2024

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