NDC 60760-658 – Ondansetron Hydrochloride

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

Human Prescription Drug

Product NDC60760-658

Product details

Brand name
Ondansetron Hydrochloride
Generic name
Ondansetron Hydrochloride
Labeler
St. Mary's Medical Park Pharmacy
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078539
Marketed since
June 20, 2023
Listing expires
December 31, 2027
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ondansetron hydrochloride →

Package NDC codes (4)

Package NDCDescriptionSince
60760-658-1010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-658-10)Jun 20, 2023
60760-658-1515 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-658-15)Sep 15, 2025
60760-658-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-658-20)Jun 23, 2025
60760-658-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-658-60)Oct 30, 2025

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