NDC 71335-0238 – Citalopram Hydrobromide

Citalopram Hydrobromide 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0238

Product details

Brand name
Citalopram Hydrobromide
Generic name
Citalopram Hydrobromide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078216
Marketed since
October 18, 2007
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Citalopram Hydrobromide →

Package NDC codes (7)

Package NDCDescriptionSince
71335-0238-130 TABLET in 1 BOTTLE (71335-0238-1)May 18, 2018
71335-0238-260 TABLET in 1 BOTTLE (71335-0238-2)Sep 19, 2018
71335-0238-390 TABLET in 1 BOTTLE (71335-0238-3)Apr 17, 2018
71335-0238-4100 TABLET in 1 BOTTLE (71335-0238-4)Jun 24, 2020
71335-0238-515 TABLET in 1 BOTTLE (71335-0238-5)Oct 30, 2024
71335-0238-6120 TABLET in 1 BOTTLE (71335-0238-6)Sep 5, 2019
71335-0238-77 TABLET in 1 BOTTLE (71335-0238-7)Oct 30, 2024

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