NDC 70518-2317 – Escitalopram

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

Human Prescription Drug

Product NDC70518-2317

Product details

Brand name
Escitalopram
Generic name
Escitalopram
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078032
Marketed since
September 9, 2019
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Escitalopram →

Package NDC codes (2)

Package NDCDescriptionSince
70518-2317-130 TABLET, FILM COATED in 1 BLISTER PACK (70518-2317-1)Nov 15, 2019
70518-2317-430 TABLET, FILM COATED in 1 BLISTER PACK (70518-2317-4)Mar 20, 2026

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