NDC 63187-513 – Ondansetron

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

Human Prescription Drug

Product NDC63187-513

Product details

Brand name
Ondansetron
Generic name
Ondansetron hydrochloride
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 (4)

Package NDCDescriptionSince
63187-513-1010 TABLET, FILM COATED in 1 BOTTLE (63187-513-10)Dec 1, 2018
63187-513-1515 TABLET, FILM COATED in 1 BOTTLE (63187-513-15)Dec 1, 2018
63187-513-2020 TABLET, FILM COATED in 1 BOTTLE (63187-513-20)Dec 1, 2018
63187-513-3030 TABLET, FILM COATED in 1 BOTTLE (63187-513-30)Dec 1, 2018

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