NDC 51655-664 – Citalopram

Citalopram Hydrobromide 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC51655-664

Product details

Brand name
Citalopram
Generic name
Citalopram
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078216
Marketed since
February 16, 2015
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for citalopram →

Package NDC codes (3)

Package NDCDescriptionSince
51655-664-2560 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (51655-664-25)Dec 10, 2020
51655-664-2690 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-664-26)Oct 19, 2023
51655-664-5230 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (51655-664-52)Feb 16, 2015

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