RxSearch

NDC properties for NDC 9 63323-305

NDC item 63323030501

NDC 963323-305
NDC 1063323-305-01
NDC Item63323030501
packaging2 mL in 1 VIAL, MULTI-DOSE
ANDAANDA065122
FDA SPL set id773621
LabelerFresenius Kabi USA, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2004-11-30
Marketing statusACTIVE

NDC item 63323030502

NDC 963323-305
NDC 1063323-305-02
NDC Item63323030502
packaging25 VIAL, MULTI-DOSE in 1 TRAY (63323-305-02) / 2 mL in 1 VIAL, MULTI-DOSE (63323-305-01)
ANDAANDA065122
FDA SPL set id773621
LabelerFresenius Kabi USA, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2004-11-30
Marketing statusACTIVE

NDC item 68083025301

NDC 968083-253
NDC 1068083-253-01
NDC Item68083025301
packaging2 mL in 1 VIAL, MULTI-DOSE
ANDAANDA209621
FDA SPL set id699468
LabelerGland Pharma Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2021-02-11
Marketing statusACTIVE

NDC item 68083025325

NDC 968083-253
NDC 1068083-253-25
NDC Item68083025325
packaging25 VIAL, MULTI-DOSE in 1 CARTON (68083-253-25) / 2 mL in 1 VIAL, MULTI-DOSE (68083-253-01)
ANDAANDA209621
FDA SPL set id699468
LabelerGland Pharma Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2021-02-11
Marketing statusACTIVE