NDC 68071-4985 – Escitalopram

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

Human Prescription Drug

Product NDC68071-4985

Product details

Brand name
Escitalopram
Generic name
Escitalopram
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202389
Marketed since
March 21, 2013
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for escitalopram →

Package NDC codes (1)

Package NDCDescriptionSince
68071-4985-330 TABLET, FILM COATED in 1 BOTTLE (68071-4985-3)Jul 25, 2019

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