NDC 62135-351 – Ondansetron

Ondansetron Hydrochloride 8 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC62135-351

Product details

Brand name
Ondansetron
Generic name
Ondansetron
Labeler
Chartwell RX, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077303
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 (2)

Package NDCDescriptionSince
62135-351-05500 TABLET in 1 BOTTLE (62135-351-05)Apr 20, 2022
62135-351-3030 TABLET in 1 BOTTLE (62135-351-30)Apr 20, 2022

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