NDC 60760-636 – Ondansetron Hydrochloride

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

Human Prescription Drug

Product NDC60760-636

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
July 31, 2007
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 (3)

Package NDCDescriptionSince
60760-636-1010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-636-10)Jul 31, 2007
60760-636-1616 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-636-16)Mar 3, 2023
60760-636-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-636-20)Mar 26, 2018

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