NDC 43063-792 – Ondansetron Hydrochloride

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

Human Prescription Drug

Product NDC43063-792

Product details

Brand name
Ondansetron Hydrochloride
Generic name
Ondansetron Hydrochloride
Labeler
PD-Rx Pharmaceuticals, Inc.
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 (1)

Package NDCDescriptionSince
43063-792-066 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-792-06)Oct 6, 2017

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