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NDC properties for NDC 9 0069-1305

NDC item 00069130501

NDC 90069-1305
NDC 100069-1305-01
NDC Item00069130501
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 00069130510

NDC 90069-1305
NDC 100069-1305-10
NDC Item00069130510
packaging10 VIAL, SINGLE-DOSE in 1 CARTON (0069-1305-10) / 1 mL in 1 VIAL, SINGLE-DOSE (0069-1305-01)
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 59353000201

NDC 959353-002
NDC 1059353-002-01
NDC Item59353000201
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 59353000210

NDC 959353-002
NDC 1059353-002-10
NDC Item59353000210
packaging10 VIAL, SINGLE-DOSE in 1 CARTON (59353-002-10) / 1 mL in 1 VIAL, SINGLE-DOSE (59353-002-01)
BLABLA125545
FDA SPL set id793734
LabelerVifor (International) Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryBLA
Marketing effective time low2018-06-18
Marketing statusACTIVE