FDA.reportPublic FDA data

Application 208872

Type
ANDA
Sponsor
AKORN

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001NALOXONE HYDROCHLORIDENALOXONE HYDROCHLORIDEINJECTABLE;INJECTION0.4MG/MLNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
17478-042Naloxone HydrochlorideNaloxone HydrochlorideAkorn, Inc.ANDACurrent
17478-042Naloxone HydrochlorideNaloxone HydrochlorideAkorn, Inc.ANDACurrent
17478-042Naloxone HydrochlorideNaloxone HydrochlorideAkorn, Inc.ANDACurrent
17478-042Naloxone HydrochlorideNaloxone HydrochlorideAkornANDACurrent
17478-042Naloxone HydrochlorideNaloxone HydrochlorideAkorn, Inc.ANDACurrent
17478-042Naloxone HydrochlorideNaloxone HydrochlorideAkornANDACurrent
17478-042Naloxone HydrochlorideNaloxone HydrochlorideAkorn, Inc.ANDACurrent
17478-042Naloxone HydrochlorideNaloxone HydrochlorideAkorn, Inc.ANDACurrent