FDA.reportPublic FDA data

Buspirone hydrochloride

Product NDC
63629-6378
11-digit product format
636296378
Labeler code
63629
Product ID
63629-6378_99e1cbdf-66d8-47e3-9478-438a39b2689d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Buspirone hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA078888
Marketing category
ANDA
Marketing start
2014-05-03
Marketing end
0000-00-00
Substance
BUSPIRONE HYDROCHLORIDE
Active strength
5 mg/1
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63629-6378-12020-05-22C16284748780-19d75b9d0-818b-f424-e053-dadaa90a57ceb2768d4e-76d3-4e6a-ab07-0d2d8da09c79
63629-6378-22020-05-22C16284748780-19d75b9d0-818b-f424-e053-dadaa90a57ceb2768d4e-76d3-4e6a-ab07-0d2d8da09c79
63629-6378-12020-01-31C16284748780-19d75b9d0-818b-f424-e053-dadaa90a57ceb2768d4e-76d3-4e6a-ab07-0d2d8da09c79
63629-6378-22020-01-31C16284748780-19d75b9d0-818b-f424-e053-dadaa90a57ceb2768d4e-76d3-4e6a-ab07-0d2d8da09c79