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NDC properties for NDC 9 76478-002

NDC item 76478000205

NDC 976478-002
NDC 1076478-002-05
NDC Item76478000205
packaging1 BOTTLE in 1 CARTON (76478-002-05) / 5 mL in 1 BOTTLE
FDA SPL set id636406
LabelerAkorn Operating Company LLC (dba Akorn)
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2014-01-02
Marketing statusACTIVE
NDANDA020439

NDC item 76478000210

NDC 976478-002
NDC 1076478-002-10
NDC Item76478000210
packaging1 BOTTLE in 1 CARTON (76478-002-10) / 10 mL in 1 BOTTLE
FDA SPL set id636406
LabelerAkorn Operating Company LLC (dba Akorn)
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2014-01-02
Marketing statusACTIVE
NDANDA020439

NDC item 76478000215

NDC 976478-002
NDC 1076478-002-15
NDC Item76478000215
packaging1 BOTTLE in 1 CARTON (76478-002-15) / 15 mL in 1 BOTTLE
FDA SPL set id636406
LabelerAkorn Operating Company LLC (dba Akorn)
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2014-01-02
Marketing statusACTIVE
NDANDA020439

NDC item 82584000205

NDC 982584-002
NDC 1082584-002-05
NDC Item82584000205
packaging1 BOTTLE, DROPPER in 1 CARTON (82584-002-05) / 5 mL in 1 BOTTLE, DROPPER
FDA SPL set id783305
LabelerThea Pharma Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2022-11-15
Marketing statusACTIVE
NDANDA020439

NDC item 82584000215

NDC 982584-002
NDC 1082584-002-15
NDC Item82584000215
packaging1 BOTTLE, DROPPER in 1 CARTON (82584-002-15) / 15 mL in 1 BOTTLE, DROPPER
FDA SPL set id783305
LabelerThea Pharma Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2022-11-15
Marketing statusACTIVE
NDANDA020439