NDC 55999-069

NDC 55999-069

NDC 55999-069 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 55999-069
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 55999-069-15 [55999006915]

Neoplex POWDER
Marketing CategoryUnapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date1985-01-01

NDC 55999-069-56 [55999006956]

Neoplex POWDER
Marketing CategoryUnapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date1985-01-01

NDC 55999-069-13 [55999006913]

Neoplex POWDER
Marketing CategoryUnapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date1985-01-01

NDC 55999-069-18 [55999006918]

Neoplex POWDER
Marketing CategoryUnapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date1985-01-01

NDC 55999-069-57 [55999006957]

Neoplex POWDER
Marketing CategoryUnapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date1985-01-01

Drug Details


© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.