Ondansetron

Product NDC
71335-0549
11-digit product format
713350549
Labeler code
71335
Product ID
71335-0549_fde9f6ab-f316-4ab6-8756-1dd76e39276c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ondansetron
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA078050
Marketing category
ANDA
Marketing start
2007-08-13
Marketing end
0000-00-00
Substance
ONDANSETRON
Active strength
8 mg/1
Pharmacologic classes
Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-0549-0713350549003 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0549-0) 2010-08-200000-00-00NoNoCurrent
71335-0549-17133505490130 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0549-1) 2010-08-200000-00-00NoNoCurrent
71335-0549-27133505490210 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0549-2) 2010-08-200000-00-00NoNoCurrent
71335-0549-3713350549035 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0549-3) 2010-08-200000-00-00NoNoCurrent
71335-0549-4713350549044 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0549-4) 2010-08-200000-00-00NoNoCurrent
71335-0549-5713350549056 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0549-5) 2010-08-200000-00-00NoNoCurrent
71335-0549-67133505490614 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0549-6) 2010-08-200000-00-00NoNoCurrent
71335-0549-77133505490760 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0549-7) 2010-08-200000-00-00NoNoCurrent
71335-0549-87133505490812 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0549-8) 2010-08-200000-00-00NoNoCurrent
71335-0549-97133505490990 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0549-9) 2010-08-200000-00-00NoNoCurrent