NDC 71205-782 – Escitalopram

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

Human Prescription Drug

Product NDC71205-782

Product details

Brand name
Escitalopram
Generic name
Escitalopram
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078032
Marketed since
March 15, 2012
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Escitalopram →

Package NDC codes (3)

Package NDCDescriptionSince
71205-782-3030 TABLET, FILM COATED in 1 BOTTLE (71205-782-30)Mar 28, 2023
71205-782-6060 TABLET, FILM COATED in 1 BOTTLE (71205-782-60)Mar 28, 2023
71205-782-9090 TABLET, FILM COATED in 1 BOTTLE (71205-782-90)Mar 28, 2023

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