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NDC properties for NDC 9 0069-1311

NDC item 00069131101

NDC 90069-1311
NDC 100069-1311-01
NDC Item00069131101
packaging1 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 00069131104

NDC 90069-1311
NDC 100069-1311-04
NDC Item00069131104
packaging4 VIAL, MULTI-DOSE in 1 CARTON (0069-1311-04) / 1 mL in 1 VIAL, MULTI-DOSE (0069-1311-01)
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 00069131110

NDC 90069-1311
NDC 100069-1311-10
NDC Item00069131110
packaging10 VIAL, MULTI-DOSE in 1 CARTON (0069-1311-10) / 1 mL in 1 VIAL, MULTI-DOSE (0069-1311-01)
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 59353012001

NDC 959353-120
NDC 1059353-120-01
NDC Item59353012001
packaging1 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 59353012010

NDC 959353-120
NDC 1059353-120-10
NDC Item59353012010
packaging10 VIAL, MULTI-DOSE in 1 CARTON (59353-120-10) / 1 mL in 1 VIAL, MULTI-DOSE (59353-120-01)
BLABLA125545
FDA SPL set id793734
LabelerVifor (International) Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryBLA
Marketing effective time low2020-09-11
Marketing statusACTIVE