ondansetron

Product NDC
68071-5230
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ondansetron
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA077557
Marketing category
ANDA
Substance
ONDANSETRON
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
68071-5230-110 TABLET, ORALLY DISINTEGRATING in 1 BOX (68071-5230-1) 2020-03-27NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
ondansetronNuCare Pharmaceuticals,Inc.2024-06-20HUMAN PRESCRIPTION DRUG LABEL3