Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1572323686
Device Listing 1572323686
Listing Summary
#
Listing key
1572323686
Premarket submission
K924827
Device
MICRODOSE POTASSIUM OXYLATE
Applicant
Unicep
Product code
LBH
Decision date
1993-03-05
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
48264
3028011
1000150986
UNICEP PACKAGING, LLC.
1
N
2020-04-25
1702 Industrial Dr SANDPOINT ID US 83864