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NDC properties for NDC 9 0069-1308

NDC item 00069130801

NDC 90069-1308
NDC 100069-1308-01
NDC Item00069130801
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 00069130810

NDC 90069-1308
NDC 100069-1308-10
NDC Item00069130810
packaging10 VIAL, SINGLE-DOSE in 1 CARTON (0069-1308-10) / 1 mL in 1 VIAL, SINGLE-DOSE (0069-1308-01)
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 59353001001

NDC 959353-010
NDC 1059353-010-01
NDC Item59353001001
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 59353001010

NDC 959353-010
NDC 1059353-010-10
NDC Item59353001010
packaging10 VIAL, SINGLE-DOSE in 1 CARTON (59353-010-10) / 1 mL in 1 VIAL, SINGLE-DOSE (59353-010-01)
BLABLA125545
FDA SPL set id793734
LabelerVifor (International) Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryBLA
Marketing effective time low2018-06-18
Marketing statusACTIVE