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NDC properties for NDC 9 0069-1306

NDC item 00069130601

NDC 90069-1306
NDC 100069-1306-01
NDC Item00069130601
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 00069130610

NDC 90069-1306
NDC 100069-1306-10
NDC Item00069130610
packaging10 VIAL, SINGLE-DOSE in 1 CARTON (0069-1306-10) / 1 mL in 1 VIAL, SINGLE-DOSE (0069-1306-01)
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 59353000301

NDC 959353-003
NDC 1059353-003-01
NDC Item59353000301
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 59353000310

NDC 959353-003
NDC 1059353-003-10
NDC Item59353000310
packaging10 VIAL, SINGLE-DOSE in 1 CARTON (59353-003-10) / 1 mL in 1 VIAL, SINGLE-DOSE (59353-003-01)
BLABLA125545
FDA SPL set id793734
LabelerVifor (International) Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryBLA
Marketing effective time low2018-06-18
Marketing statusACTIVE