NDC 51655-016 – Ondansetron Hydrochloride

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

Human Prescription Drug

Product NDC51655-016

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
August 8, 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 (4)

Package NDCDescriptionSince
51655-016-2712 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-27)Sep 16, 2022
51655-016-5310 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-53)Sep 16, 2022
51655-016-5415 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-54)Aug 8, 2022
51655-016-876 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-87)Sep 21, 2022

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