NDC 82804-257 – Ondansetron Hydrochloride

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

Human Prescription Drug

Product NDC82804-257

Product details

Brand name
Ondansetron Hydrochloride
Generic name
Ondansetron Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078539
Marketed since
July 31, 2007
Listing expires
December 31, 2027
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
82804-257-1010 TABLET, FILM COATED in 1 BOTTLE (82804-257-10)Jun 23, 2026
82804-257-1515 TABLET, FILM COATED in 1 BOTTLE (82804-257-15)Aug 27, 2026
82804-257-3030 TABLET, FILM COATED in 1 BOTTLE (82804-257-30)Jul 15, 2026

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