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NDC properties for NDC 9 39822-0706

NDC item 39822070601

NDC 939822-0706
NDC 1039822-0706-1
NDC Item39822070601
packaging1 in 1 VIAL
ANDAANDA064210
FDA SPL set id725208
LabelerXGen Pharmaceuticals DJB, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low1998-06-30
Marketing statusACTIVE

NDC item 39822070602

NDC 939822-0706
NDC 1039822-0706-2
NDC Item39822070602
packaging10 VIAL in 1 BOX (39822-0706-2) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (39822-0706-1)
ANDAANDA064210
FDA SPL set id725208
LabelerXGen Pharmaceuticals DJB, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low1998-06-30
Marketing statusACTIVE