FDA.reportPublic FDA data

Application 083246

Type
ANDA
Sponsor
OAK PHARMS

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001NEMBUTAL SODIUMPENTOBARBITAL SODIUMINJECTABLE;INJECTION50MG/MLNoYes

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
17478-181Pentobarbital SodiumPentobarbital SodiumAkorn, Inc.ANDACurrent
17478-181Pentobarbital SodiumPentobarbital SodiumAkornANDACurrent
17478-181Pentobarbital SodiumPentobarbital SodiumAkornANDACurrent
17478-181Pentobarbital SodiumPentobarbital SodiumAkorn, Inc.ANDACurrent
17478-181Pentobarbital SodiumPentobarbital SodiumAkorn, Inc.ANDACurrent
17478-181Pentobarbital SodiumPentobarbital SodiumAkorn, Inc.ANDACurrent
17478-181Pentobarbital SodiumPentobarbital SodiumAkornANDACurrent
76478-501Nembutal Sodiumpentobarbital sodiumAkronANDACurrent
76478-501Nembutal Sodiumpentobarbital sodiumOak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.)ANDACurrent
76478-501Nembutal Sodiumpentobarbital sodiumOak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.)ANDACurrent
76478-501Nembutal Sodiumpentobarbital sodiumOak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.)ANDACurrent
76478-501Nembutal Sodiumpentobarbital sodiumOak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.)ANDACurrent
76478-501Nembutal Sodiumpentobarbital sodiumAkronANDACurrent