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NDC properties for NDC 9 17478-604

NDC item 17478060400

NDC 917478-604
NDC 1017478-604-00
NDC Item17478060400
packaging0.2 mL in 1 VIAL, SINGLE-USE
packaging15 in 1 POUCH
FDA SPL set id636466
LabelerAkorn Operating Company LLC (dba Akorn)
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2014-05-14
Marketing statusACTIVE
NDANDA202667

NDC item 17478060401

NDC 917478-604
NDC 1017478-604-01
NDC Item17478060401
packaging0.2 mL in 1 VIAL, SINGLE-USE
packaging15 in 1 POUCH
FDA SPL set id636466
LabelerAkorn Operating Company LLC (dba Akorn)
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2014-05-14
Marketing statusACTIVE
NDANDA202667

NDC item 17478060430

NDC 917478-604
NDC 1017478-604-30
NDC Item17478060430
packaging4 POUCH in 1 CARTON (17478-604-30) / 15 VIAL, SINGLE-USE in 1 POUCH (17478-604-01) / .2 mL in 1 VIAL, SINGLE-USE
FDA SPL set id636466
LabelerAkorn Operating Company LLC (dba Akorn)
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2014-05-14
Marketing statusACTIVE
NDANDA202667

NDC item 82584060401

NDC 982584-604
NDC 1082584-604-01
NDC Item82584060401
packaging0.2 mL in 1 VIAL, SINGLE-DOSE
packaging15 in 1 POUCH
FDA SPL set id761201
LabelerThea Pharma Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2022-12-10
Marketing statusACTIVE
NDANDA202667

NDC item 82584060430

NDC 982584-604
NDC 1082584-604-30
NDC Item82584060430
packaging4 POUCH in 1 CARTON (82584-604-30) / 15 VIAL, SINGLE-DOSE in 1 POUCH (82584-604-01) / .2 mL in 1 VIAL, SINGLE-DOSE
FDA SPL set id761201
LabelerThea Pharma Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2022-12-10
Marketing statusACTIVE
NDANDA202667