Ondansetron

Product NDC
71335-9726
11-digit product format
713359726
Labeler code
71335
Product ID
71335-9726_312be717-1f36-4d21-a99c-0a125764618a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ondansetron
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA078152
Marketing category
ANDA
Marketing start
2007-06-27
Substance
ONDANSETRON
Active strength
4 mg/1
Pharmacologic classes
Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
4AF302ESOSONDANSETRON99614-02-5ONDANSETRON

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71335-9726-07133597260090 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-0) 2023-05-30NoNoHistorical
71335-9726-17133597260130 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-1) 2023-05-30NoNoHistorical
71335-9726-27133597260220 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-2) 2023-05-30NoNoHistorical
71335-9726-37133597260310 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-3) 2023-05-30NoNoHistorical
71335-9726-4713359726046 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-4) 2023-05-30NoNoHistorical
71335-9726-57133597260560 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-5) 2023-05-30NoNoHistorical
71335-9726-6713359726069 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-6) 2023-05-30NoNoHistorical
71335-9726-7713359726075 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-7) 2023-05-30NoNoHistorical
71335-9726-87133597260815 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-8) 2023-05-30NoNoHistorical
71335-9726-9713359726093 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-9) 2023-05-30NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
OndansetronBryant Ranch Prepack2024-08-08HUMAN PRESCRIPTION DRUG LABEL102