NDC 48106-1167

NDC 48106-1167

NDC 48106-1167 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 48106-1167
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 48106-1167-5 [48106116705]

Dermaplex LIQUID
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2007-08-01

NDC 48106-1167-7 [48106116707]

Dermaplex LIQUID
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2007-08-01

NDC 48106-1167-1 [48106116701]

Dermaplex LIQUID
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2007-08-01

NDC 48106-1167-3 [48106116703]

Dermaplex LIQUID
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2007-08-01

NDC 48106-1167-2 [48106116702]

Dermaplex LIQUID
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2007-08-01

NDC 48106-1167-6 [48106116706]

Dermaplex LIQUID
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2007-08-01

Drug Details


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