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NDC properties for NDC 9 0069-1307

NDC item 00069130701

NDC 90069-1307
NDC 100069-1307-01
NDC Item00069130701
packaging1 mL in 1 VIAL, SINGLE-DOSE
BLABLA125545
FDA SPL set id792529
LabelerPfizer Laboratories Div Pfizer Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryBLA
Marketing effective time low2018-06-18
Marketing statusACTIVE

NDC item 00069130710

NDC 90069-1307
NDC 100069-1307-10
NDC Item00069130710
packaging10 VIAL, SINGLE-DOSE in 1 CARTON (0069-1307-10) / 1 mL in 1 VIAL, SINGLE-DOSE (0069-1307-01)
BLABLA125545
FDA SPL set id792529
LabelerPfizer Laboratories Div Pfizer Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryBLA
Marketing effective time low2018-06-18
Marketing statusACTIVE

NDC item 59353000401

NDC 959353-004
NDC 1059353-004-01
NDC Item59353000401
packaging1 mL in 1 VIAL, SINGLE-DOSE
BLABLA125545
FDA SPL set id793734
LabelerVifor (International) Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryBLA
Marketing effective time low2018-06-18
Marketing statusACTIVE

NDC item 59353000410

NDC 959353-004
NDC 1059353-004-10
NDC Item59353000410
packaging10 VIAL, SINGLE-DOSE in 1 CARTON (59353-004-10) / 1 mL in 1 VIAL, SINGLE-DOSE (59353-004-01)
BLABLA125545
FDA SPL set id793734
LabelerVifor (International) Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryBLA
Marketing effective time low2018-06-18
Marketing statusACTIVE