NDC 71335-0685 – Escitalopram oxalate

Escitalopram Oxalate 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0685

Product details

Brand name
Escitalopram oxalate
Generic name
Escitalopram oxalate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090939
Marketed since
September 11, 2012
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

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

Package NDC codes (8)

Package NDCDescriptionSince
71335-0685-160 TABLET in 1 BOTTLE (71335-0685-1)Feb 27, 2018
71335-0685-228 TABLET in 1 BOTTLE (71335-0685-2)Oct 30, 2024
71335-0685-330 TABLET in 1 BOTTLE (71335-0685-3)Feb 22, 2018
71335-0685-490 TABLET in 1 BOTTLE (71335-0685-4)Feb 12, 2018
71335-0685-5120 TABLET in 1 BOTTLE (71335-0685-5)Oct 30, 2024
71335-0685-6100 TABLET in 1 BOTTLE (71335-0685-6)Oct 30, 2024
71335-0685-745 TABLET in 1 BOTTLE (71335-0685-7)Oct 30, 2024
71335-0685-8180 TABLET in 1 BOTTLE (71335-0685-8)Oct 30, 2024

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