busPIRone HCl

Product NDC
71335-1390
11-digit product format
713351390
Labeler code
71335
Product ID
71335-1390_696c5626-6387-4856-b2bb-b890d5a3123b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
buspirone hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA208829
Marketing category
ANDA
Marketing start
2017-05-24
Marketing end
0000-00-00
Substance
BUSPIRONE HYDROCHLORIDE
Active strength
30 mg/1
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1390-17133513900160 TABLET in 1 BOTTLE (71335-1390-1) 60 tablet2019-11-110000-00-00NoNoCurrent
71335-1390-27133513900230 TABLET in 1 BOTTLE (71335-1390-2) 30 tablet2019-11-110000-00-00NoNoCurrent
71335-1390-37133513900356 TABLET in 1 BOTTLE (71335-1390-3) 56 tablet2019-11-110000-00-00NoNoCurrent
71335-1390-47133513900490 TABLET in 1 BOTTLE (71335-1390-4) 90 tablet2019-11-110000-00-00NoNoCurrent
71335-1390-571335139005180 TABLET in 1 BOTTLE (71335-1390-5) 180 tablet2019-11-110000-00-00NoNoCurrent
71335-1390-67133513900615 TABLET in 1 BOTTLE (71335-1390-6) 15 tablet2019-11-110000-00-00NoNoCurrent
71335-1390-771335139007120 TABLET in 1 BOTTLE (71335-1390-7) 120 tablet2021-12-280000-00-00NoNoCurrent