NDC 68569-101

NDC 68569-101

NDC 68569-101 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 68569-101
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 68569-101-08 [68569010108]

KENOSTART LIQUID
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2014-07-30

NDC 68569-101-06 [68569010106]

KENOSTART LIQUID
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2014-07-30

NDC 68569-101-07 [68569010107]

KENOSTART LIQUID
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2014-07-30

NDC 68569-101-02 [68569010102]

KENOSTART LIQUID
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2014-07-30

NDC 68569-101-01 [68569010101]

KENOSTART LIQUID
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2014-07-30

NDC 68569-101-05 [68569010105]

KENOSTART LIQUID
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2014-07-30

NDC 68569-101-03 [68569010103]

KENOSTART LIQUID
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2014-07-30

NDC 68569-101-04 [68569010104]

KENOSTART LIQUID
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2014-07-30

NDC 68569-101-09 [68569010109]

KENOSTART LIQUID
Marketing Categoryunapproved drug other
Product TypeOTC ANIMAL DRUG
Marketing Start Date2014-07-30

Drug Details

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