NDC 61919-565 – Ondansetron

Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC61919-565

Product details

Brand name
Ondansetron
Generic name
Ondansetron
Labeler
Direct_Rx
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078539
Marketed since
August 22, 2019
Listing expires
December 31, 2027
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ondansetron →

Package NDC codes (2)

Package NDCDescriptionSince
61919-565-3030 TABLET, FILM COATED in 1 BOTTLE (61919-565-30)Aug 22, 2019
61919-565-4545 TABLET, FILM COATED in 1 BOTTLE (61919-565-45)Aug 22, 2019

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