NDC 0378-6233 – Citalopram

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

Human Prescription Drug 1 recall

Product NDC0378-6233

Product details

Brand name
Citalopram
Generic name
Citalopram
Labeler
Mylan Pharmaceuticals Inc.
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 (2)

Package NDCDescriptionSince
0378-6233-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6233-01)Jul 28, 2008
0378-6233-05500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6233-05)Jul 28, 2008

Recalls mentioning this NDC

Other Citalopram products