ondansetron

Product NDC
55154-3551
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ondansetron hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Cardinal Health 107, LLC
Application
ANDA076183
Marketing category
ANDA
Substance
ONDANSETRON HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
55154-3551-010 BLISTER PACK in 1 BAG (55154-3551-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK2025-05-05NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
ondansetronCardinal Health 107, LLC2026-01-12HUMAN PRESCRIPTION DRUG LABEL6