NDC 53746-020 – Escitalopram Oxalate

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

Human Prescription Drug

Product NDC53746-020

Product details

Brand name
Escitalopram Oxalate
Generic name
Escitalopram Oxalate
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205619
Marketed since
May 17, 2017
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
53746-020-05500 TABLET, FILM COATED in 1 BOTTLE (53746-020-05)May 17, 2017
53746-020-101000 TABLET, FILM COATED in 1 BOTTLE (53746-020-10)May 17, 2017
53746-020-3030 TABLET, FILM COATED in 1 BOTTLE (53746-020-30)May 17, 2017
53746-020-9090 TABLET, FILM COATED in 1 BOTTLE (53746-020-90)May 17, 2017

Other Escitalopram oxalate products