FDA
.report
PMA
PMN
De Novo
MAUDE
GUDID
NDC
DailyMed
Drug Applications
NDC 51098-501
NDC 51098-501
NDC 51098-501 is a in the
category. It is labeled and distributed by .
Proprietary Name
NDC 51098-501
Marketing Category
/
Packaging
NDC SPL Data Element Entries
NDC 51098-501-01 [51098050101]
Allantoin .4% LIQUID
Marketing Category
unapproved drug other
Product Type
OTC ANIMAL DRUG
Marketing Start Date
2013-10-01
Drug Details
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.