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NDC properties for NDC 9 0069-1318

NDC item 00069131801

NDC 90069-1318
NDC 100069-1318-01
NDC Item00069131801
packaging2 mL in 1 VIAL, MULTI-DOSE
BLABLA125545
FDA SPL set id792529
LabelerPfizer Laboratories Div Pfizer Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryBLA
Marketing effective time low2020-11-09
Marketing statusACTIVE

NDC item 00069131804

NDC 90069-1318
NDC 100069-1318-04
NDC Item00069131804
packaging4 VIAL, MULTI-DOSE in 1 CARTON (0069-1318-04) / 2 mL in 1 VIAL, MULTI-DOSE (0069-1318-01)
BLABLA125545
FDA SPL set id792529
LabelerPfizer Laboratories Div Pfizer Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryBLA
Marketing effective time low2020-11-09
Marketing statusACTIVE

NDC item 00069131810

NDC 90069-1318
NDC 100069-1318-10
NDC Item00069131810
packaging10 VIAL, MULTI-DOSE in 1 CARTON (0069-1318-10) / 2 mL in 1 VIAL, MULTI-DOSE (0069-1318-01)
BLABLA125545
FDA SPL set id792529
LabelerPfizer Laboratories Div Pfizer Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryBLA
Marketing effective time low2020-11-09
Marketing statusACTIVE

NDC item 59353022001

NDC 959353-220
NDC 1059353-220-01
NDC Item59353022001
packaging2 mL in 1 VIAL, MULTI-DOSE
BLABLA125545
FDA SPL set id793734
LabelerVifor (International) Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryBLA
Marketing effective time low2020-09-11
Marketing statusACTIVE

NDC item 59353022010

NDC 959353-220
NDC 1059353-220-10
NDC Item59353022010
packaging10 VIAL, MULTI-DOSE in 1 CARTON (59353-220-10) / 2 mL in 1 VIAL, MULTI-DOSE (59353-220-01)
BLABLA125545
FDA SPL set id793734
LabelerVifor (International) Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryBLA
Marketing effective time low2020-09-11
Marketing statusACTIVE