NDC 51655-933 – Ondansetron Hydrochloride

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

Human Prescription Drug

Product NDC51655-933

Product details

Brand name
Ondansetron Hydrochloride
Generic name
Ondansetron Hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078539
Marketed since
July 20, 2022
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 (6)

Package NDCDescriptionSince
51655-933-044 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-04)Oct 25, 2022
51655-933-433 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-43)Jul 20, 2022
51655-933-5310 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-53)Sep 16, 2022
51655-933-5415 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-54)May 11, 2023
51655-933-555 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-55)May 9, 2023
51655-933-876 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-87)Jul 20, 2022

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