Buspirone Hydrochloride

Product NDC
63629-7277
11-digit product format
636297277
Labeler code
63629
Product ID
63629-7277_bdc628c1-d777-42fc-8883-7cdc6b93b465
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Buspirone Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA202557
Marketing category
ANDA
Marketing start
2016-11-14
Marketing end
0000-00-00
Substance
BUSPIRONE HYDROCHLORIDE
Active strength
8 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
63629-7277-16362972770130 TABLET in 1 BOTTLE (63629-7277-1) 30 tablet2022-03-080000-00-00NoNoCurrent
63629-7277-26362972770290 TABLET in 1 BOTTLE (63629-7277-2) 90 tablet2017-05-080000-00-00NoNoCurrent
63629-7277-36362972770318 TABLET in 1 BOTTLE (63629-7277-3) 18 tablet2022-03-080000-00-00NoNoCurrent
63629-7277-46362972770428 TABLET in 1 BOTTLE (63629-7277-4) 28 tablet2022-03-080000-00-00NoNoCurrent
63629-7277-56362972770560 TABLET in 1 BOTTLE (63629-7277-5) 60 tablet2018-02-280000-00-00NoNoCurrent
63629-7277-663629727706120 TABLET in 1 BOTTLE (63629-7277-6) 120 tablet2022-03-080000-00-00NoNoCurrent