NDC 0615-8022 – Citalopram

Citalopram Hydrobromide 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0615-8022

Product details

Brand name
Citalopram
Generic name
Citalopram Hydrobromide
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077031
Marketed since
October 28, 2004
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Citalopram →

Package NDC codes (2)

Package NDCDescriptionSince
0615-8022-0515 TABLET, FILM COATED in 1 BLISTER PACK (0615-8022-05)Oct 28, 2004
0615-8022-3930 TABLET, FILM COATED in 1 BLISTER PACK (0615-8022-39)Oct 28, 2004

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