NDC 54348-819 – Ondansetron

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

Human Prescription Drug

Product NDC54348-819

Product details

Brand name
Ondansetron
Generic name
Ondansetron
Labeler
PharmPak, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078539
Marketed since
July 10, 2019
Listing expires
December 31, 2026
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ondansetron →

Package NDC codes (5)

Package NDCDescriptionSince
54348-819-001 BOTTLE in 1 BOX (54348-819-00) / 1 TABLET, FILM COATED in 1 BOTTLEJul 10, 2019
54348-819-021 BOTTLE in 1 BOX (54348-819-02) / 2 TABLET, FILM COATED in 1 BOTTLEJul 10, 2019
54348-819-041 BOTTLE in 1 BOX (54348-819-04) / 4 TABLET, FILM COATED in 1 BOTTLEJul 10, 2019
54348-819-061 BOTTLE in 1 BOX (54348-819-06) / 6 TABLET, FILM COATED in 1 BOTTLEJul 10, 2019
54348-819-081 BOTTLE in 1 BOX (54348-819-08) / 8 TABLET, FILM COATED in 1 BOTTLEJul 10, 2019

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