NDC 55756-062

NDC 55756-062

NDC 55756-062 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 55756-062
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 55756-062-01 [55756006201]

OceanBlu Pre-Post SOLUTION
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2014-11-01

NDC 55756-062-27 [55756006227]

OceanBlu Pre-Post SOLUTION
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2018-01-15

NDC 55756-062-23 [55756006223]

OceanBlu Pre-Post SOLUTION
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2018-01-15

NDC 55756-062-02 [55756006202]

OceanBlu Pre-Post SOLUTION
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2014-11-01

NDC 55756-062-08 [55756006208]

OceanBlu Pre-Post SOLUTION
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2018-01-15

Drug Details


© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.