NDC 71610-119 – Ondansetron Hydrochloride

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

Human Prescription Drug

Product NDC71610-119

Product details

Brand name
Ondansetron Hydrochloride
Generic name
Ondansetron Hydrochloride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
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 (1)

Package NDCDescriptionSince
71610-119-88900 TABLET, FILM COATED in 1 BOTTLE (71610-119-88)Aug 15, 2018

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