NDC 71610-534 – Escitalopram oxalate

Escitalopram Oxalate 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71610-534

Product details

Brand name
Escitalopram oxalate
Generic name
Escitalopram
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078604
Marketed since
October 1, 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 (1)

Package NDCDescriptionSince
71610-534-6090 TABLET, FILM COATED in 1 BOTTLE (71610-534-60)Mar 9, 2021

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