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NDC properties for NDC 9 0703-4636

NDC item 00703463601

NDC 90703-4636
NDC 100703-4636-01
NDC Item00703463601
packaging10 mL in 1 VIAL (0703-4636-01)
FDA SPL set id717032
LabelerTeva Parenteral Medicines, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2003-12-03
Marketing statusACTIVE
NDANDA050577

NDC item 26060953004

NDC 926060-9530
NDC 1026060-9530-4
NDC Item26060953004

NDC item 68118010001

NDC 968118-100
NDC 1068118-100-01
NDC Item68118010001
packaging1 VIAL, GLASS in 1 CARTON (68118-100-01) / 10 mL in 1 VIAL, GLASS
FDA SPL set id704547
LabelerESTEVE PHARMACEUTICALS, S.A.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryUNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Marketing effective time low2023-02-01
Marketing statusACTIVE
UNAPPROVED_DRUG_FOR_USE_IN_DRUG_SHORTAGEN/A