NDC 50090-3185 – Ondansetron Hydrochloride

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

Human Prescription Drug

Product NDC50090-3185

Product details

Brand name
Ondansetron Hydrochloride
Generic name
Ondansetron Hydrochloride
Labeler
A-S Medication Solutions
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 (5)

Package NDCDescriptionSince
50090-3185-04 TABLET, FILM COATED in 1 BOTTLE (50090-3185-0)Jan 17, 2018
50090-3185-110 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3185-1)Nov 28, 2014
50090-3185-23 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3185-2)Nov 28, 2014
50090-3185-330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3185-3)Nov 28, 2014
50090-3185-46 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3185-4)Nov 28, 2014

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