NDC 68001-591 – Escitalopram

Escitalopram Oxalate 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68001-591

Product details

Brand name
Escitalopram
Generic name
Escitalopram
Labeler
BluePoint Laboratories
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078032
Marketed since
December 18, 2023
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Escitalopram →

Package NDC codes (1)

Package NDCDescriptionSince
68001-591-00100 TABLET, FILM COATED in 1 BOTTLE (68001-591-00)Dec 18, 2023

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