NDC 63187-065 – Ondansetron

Ondansetron Hydrochloride 8 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC63187-065

Product details

Brand name
Ondansetron
Generic name
Ondansetron
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077851
Marketed since
June 25, 2007
Listing expires
December 31, 2026
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ondansetron →

Package NDC codes (6)

Package NDCDescriptionSince
63187-065-1010 TABLET, FILM COATED in 1 BOTTLE (63187-065-10)Apr 1, 2014
63187-065-1515 TABLET, FILM COATED in 1 BOTTLE (63187-065-15)Apr 1, 2014
63187-065-2020 TABLET, FILM COATED in 1 BOTTLE (63187-065-20)Apr 1, 2014
63187-065-3030 TABLET, FILM COATED in 1 BOTTLE (63187-065-30)Apr 1, 2014
63187-065-6060 TABLET, FILM COATED in 1 BOTTLE (63187-065-60)Apr 1, 2014
63187-065-9090 TABLET, FILM COATED in 1 BOTTLE (63187-065-90)Apr 1, 2014

Other Ondansetron products