NDC 58597-8135

NDC 58597-8135

NDC 58597-8135 is a in the category. It is labeled and distributed by American Pharmaceutical Ingredients Llc.

Product ID58597-8135_93e55c71-b9b2-4448-8abd-870b7931654c
NDC58597-8135
Proprietary NameNDC 58597-8135
Marketing Start Date2014-04-16
Marketing Category/
Labeler NameAMERICAN PHARMACEUTICAL INGREDIENTS LLC

Packaging

NDC 58597-8135-2

4000 g in 1 BOTTLE (58597-8135-2)
NDC Exclude FlagN
Sample Package?N

Drug Details

Active Ingredients

IngredientStrength
BENZYL ALCOHOL1 g/g

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