NDC 55700-631 – Ondansetron Hydrochloride

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

Human Prescription Drug

Product NDC55700-631

Product details

Brand name
Ondansetron Hydrochloride
Generic name
Ondansetron Hydrochloride
Labeler
Quality Care Products LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078539
Marketed since
May 25, 2018
Marketing end
January 31, 2028
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
55700-631-1010 TABLET, FILM COATED in 1 BOTTLE (55700-631-10)May 25, 2018
55700-631-2020 TABLET, FILM COATED in 1 BOTTLE (55700-631-20)May 25, 2018
55700-631-3030 TABLET, FILM COATED in 1 BOTTLE (55700-631-30)May 25, 2018

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