NDC 71205-744 – Ondansetron Hydrochloride

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

Human Prescription Drug

Product NDC71205-744

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, 2026
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

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

Package NDC codes (7)

Package NDCDescriptionSince
71205-744-1010 TABLET, FILM COATED in 1 BOTTLE (71205-744-10)Jan 16, 2023
71205-744-1212 TABLET, FILM COATED in 1 BOTTLE (71205-744-12)Jun 13, 2023
71205-744-1515 TABLET, FILM COATED in 1 BOTTLE (71205-744-15)Jan 16, 2023
71205-744-2020 TABLET, FILM COATED in 1 BOTTLE (71205-744-20)Jan 16, 2023
71205-744-3030 TABLET, FILM COATED in 1 BOTTLE (71205-744-30)Jan 16, 2023
71205-744-6060 TABLET, FILM COATED in 1 BOTTLE (71205-744-60)Jan 16, 2023
71205-744-9090 TABLET, FILM COATED in 1 BOTTLE (71205-744-90)Jan 16, 2023

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