NDC 65862-007 – Citalopram

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

Human Prescription Drug

Product NDC65862-007

Product details

Brand name
Citalopram
Generic name
Citalopram Hydrobromide
Labeler
Aurobindo Pharma Limited
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 (7)

Package NDCDescriptionSince
65862-007-01100 TABLET, FILM COATED in 1 BOTTLE (65862-007-01)Oct 28, 2004
65862-007-05500 TABLET, FILM COATED in 1 BOTTLE (65862-007-05)Oct 28, 2004
65862-007-1010 BLISTER PACK in 1 CARTON (65862-007-10) / 10 TABLET, FILM COATED in 1 BLISTER PACKOct 28, 2004
65862-007-3030 TABLET, FILM COATED in 1 BOTTLE (65862-007-30)Oct 28, 2004
65862-007-3230 TABLET, FILM COATED in 1 BLISTER PACK (65862-007-32)Oct 28, 2004
65862-007-6060 TABLET, FILM COATED in 1 BOTTLE (65862-007-60)Oct 28, 2004
65862-007-9090 TABLET, FILM COATED in 1 BOTTLE (65862-007-90)Oct 28, 2004

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