NDC 69097-847 – Escitalopram Oxalate

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

Human Prescription Drug

Product NDC69097-847

Product details

Brand name
Escitalopram Oxalate
Generic name
Escitalopram
Labeler
Cipla USA Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078604
Marketed since
June 16, 2016
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Escitalopram oxalate →

Package NDC codes (5)

Package NDCDescriptionSince
69097-847-0230 TABLET, FILM COATED in 1 BOTTLE (69097-847-02)Jun 16, 2016
69097-847-0590 TABLET, FILM COATED in 1 BOTTLE (69097-847-05)Jun 16, 2016
69097-847-07100 TABLET, FILM COATED in 1 BOTTLE (69097-847-07)Jun 16, 2016
69097-847-12500 TABLET, FILM COATED in 1 BOTTLE (69097-847-12)Jun 16, 2016
69097-847-151000 TABLET, FILM COATED in 1 BOTTLE (69097-847-15)Jun 16, 2016

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