Buspirone Hydrochloride

Product NDC
63629-1747
11-digit product format
636291747
Labeler code
63629
Product ID
63629-1747_d478fe31-e339-48e7-82da-f29199389d8a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Buspirone Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA075022
Marketing category
ANDA
Marketing start
2002-03-01
Marketing end
0000-00-00
Substance
BUSPIRONE HYDROCHLORIDE
Active strength
15 mg/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-1747-1EA - Each63629-1747d5c42f2d-b210-46ce-9dfa-4826a24a021312013-02-13
63629-1747-2EA - Each63629-1747605952ca-7d61-4d8d-bfd6-43c19267e60012013-02-13
63629-1747-3EA - Each63629-17476ffd466d-2e50-42bc-82d4-bc6697916b7e12013-02-13
63629-1747-4EA - Each63629-1747e863949e-bbf3-4331-b699-2f6981d853ab12013-02-13