NDC 65862-187 – Ondansetron Hydrochloride

Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC65862-187

Product details

Brand name
Ondansetron Hydrochloride
Generic name
Ondansetron Hydrochloride
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078539
Marketed since
July 31, 2007
Listing expires
December 31, 2026
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ondansetron hydrochloride →

Package NDC codes (5)

Package NDCDescriptionSince
65862-187-031 BLISTER PACK in 1 CARTON (65862-187-03) / 3 TABLET, FILM COATED in 1 BLISTER PACKJul 31, 2007
65862-187-05500 TABLET, FILM COATED in 1 BOTTLE (65862-187-05)Jul 31, 2007
65862-187-1010 BLISTER PACK in 1 CARTON (65862-187-10) / 10 TABLET, FILM COATED in 1 BLISTER PACKJul 31, 2007
65862-187-3030 TABLET, FILM COATED in 1 BOTTLE (65862-187-30)Jul 31, 2007
65862-187-991000 TABLET, FILM COATED in 1 BOTTLE (65862-187-99)Jul 31, 2007

Recalls mentioning this NDC

Other Ondansetron hydrochloride products