NDC 68071-3069 – Escitalopram

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

Human Prescription Drug

Product NDC68071-3069

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 (2)

Package NDCDescriptionSince
68071-3069-330 TABLET, FILM COATED in 1 BOTTLE (68071-3069-3)Mar 10, 2017
68071-3069-828 TABLET, FILM COATED in 1 BOTTLE (68071-3069-8)Mar 10, 2017

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