NDC 51655-415 – Ondansetron Hydrochloride

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

Human Prescription Drug

Product NDC51655-415

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
December 7, 2017
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
51655-415-044 TABLET, FILM COATED in 1 BOTTLE (51655-415-04)Apr 12, 2018
51655-415-433 TABLET, FILM COATED in 1 BOTTLE (51655-415-43)Dec 28, 2017
51655-415-5310 TABLET, FILM COATED in 1 BOTTLE (51655-415-53)Apr 24, 2018
51655-415-5415 TABLET, FILM COATED in 1 BOTTLE (51655-415-54)Dec 28, 2017
51655-415-555 TABLET, FILM COATED in 1 BOTTLE (51655-415-55)Dec 7, 2017
51655-415-876 TABLET, FILM COATED in 1 BOTTLE (51655-415-87)Oct 24, 2018

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