NDC 71335-2232 – Citalopram

Citalopram Hydrobromide 40 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2232

Product details

Brand name
Citalopram
Generic name
Citalopram
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077042
Marketed since
July 28, 2008
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Citalopram →

Package NDC codes (6)

Package NDCDescriptionSince
71335-2232-130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-1)Sep 18, 2023
71335-2232-240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-2)Oct 4, 2024
71335-2232-360 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-3)Oct 4, 2024
71335-2232-490 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-4)Sep 18, 2023
71335-2232-5100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-5)Oct 4, 2024
71335-2232-6180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-6)Oct 4, 2024

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