NDC 63304-459 – Ondansetron

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

Human Prescription Drug

Product NDC63304-459

Product details

Brand name
Ondansetron
Generic name
Ondansetron
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077851
Marketed since
June 25, 2007
Listing expires
December 31, 2026
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ondansetron →

Package NDC codes (1)

Package NDCDescriptionSince
63304-459-3030 TABLET, FILM COATED in 1 BOTTLE (63304-459-30)Jun 25, 2007

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