NDC 0615-8185 – Ondansetron hydrochloride

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

Human Prescription Drug

Product NDC0615-8185

Product details

Brand name
Ondansetron hydrochloride
Generic name
Ondansetron hydrochloride
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076183
Marketed since
December 26, 2006
Listing expires
December 31, 2026
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
0615-8185-005 TABLET, FILM COATED in 1 BLISTER PACK (0615-8185-00)Apr 22, 2024
0615-8185-0515 TABLET, FILM COATED in 1 BLISTER PACK (0615-8185-05)Mar 24, 2020
0615-8185-1010 TABLET, FILM COATED in 1 BLISTER PACK (0615-8185-10)Nov 7, 2018
0615-8185-1212 TABLET, FILM COATED in 1 BLISTER PACK (0615-8185-12)Jan 26, 2024
0615-8185-3930 TABLET, FILM COATED in 1 BLISTER PACK (0615-8185-39)Nov 7, 2018

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