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NDC properties for NDC 9 0143-9375

NDC item 00143937501

NDC 90143-9375
NDC 100143-9375-01
NDC Item00143937501
packaging1 mL in 1 VIAL
ANDAANDA078630
FDA SPL set id651710
LabelerHikma Pharmaceuticals USA Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2009-05-20
Marketing statusACTIVE

NDC item 00143937510

NDC 90143-9375
NDC 100143-9375-10
NDC Item00143937510
packaging10 VIAL in 1 CARTON (0143-9375-10) / 1 mL in 1 VIAL (0143-9375-01)
ANDAANDA078630
FDA SPL set id651710
LabelerHikma Pharmaceuticals USA Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2009-05-20
Marketing statusACTIVE

NDC item 00143974601

NDC 90143-9746
NDC 100143-9746-01
NDC Item00143974601
packaging1 mL in 1 VIAL
ANDAANDA078630
FDA SPL set id760353
LabelerHikma Pharmaceuticals USA Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2009-05-20
Marketing statusACTIVE

NDC item 00143974610

NDC 90143-9746
NDC 100143-9746-10
NDC Item00143974610
packaging10 VIAL in 1 CARTON (0143-9746-10) / 1 mL in 1 VIAL (0143-9746-01)
ANDAANDA078630
FDA SPL set id760353
LabelerHikma Pharmaceuticals USA Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2009-05-20
Marketing statusACTIVE

NDC item 00404996201

NDC 90404-9962
NDC 100404-9962-01
NDC Item00404996201
packaging1 VIAL in 1 BAG (0404-9962-01) / 1 mL in 1 VIAL
ANDAANDA076887
FDA SPL set id711310
LabelerHenry Schein, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-01-12
Marketing statusACTIVE

NDC item 55390010110

NDC 955390-101
NDC 1055390-101-10
NDC Item55390010110
packaging10 VIAL in 1 BOX (55390-101-10) / 1 mL in 1 VIAL
ANDAANDA076770
FDA SPL set id17160
LabelerBedford Laboratories
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2011-12-31
Marketing effective time low2004-04-28
Marketing statusCOMPLETED

NDC item 63323066500

NDC 963323-665
NDC 1063323-665-00
NDC Item63323066500
packaging1 mL in 1 VIAL, SINGLE-USE
ANDAANDA076887
FDA SPL set id650769
LabelerFresenius Kabi USA, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2011-03-10
Marketing statusACTIVE

NDC item 63323066501

NDC 963323-665
NDC 1063323-665-01
NDC Item63323066501
packaging25 VIAL, SINGLE-USE in 1 TRAY (63323-665-01) / 1 mL in 1 VIAL, SINGLE-USE (63323-665-00)
ANDAANDA076887
FDA SPL set id650769
LabelerFresenius Kabi USA, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2011-03-10
Marketing statusACTIVE

NDC item 70860080101

NDC 970860-801
NDC 1070860-801-01
NDC Item70860080101
packaging10 VIAL in 1 CARTON (70860-801-01) / 1 mL in 1 VIAL (70860-801-41)
ANDAANDA200122
FDA SPL set id353618
LabelerAthenex Pharmaceutical Division, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2020-08-31
Marketing effective time low2017-02-22
Marketing statusCOMPLETED

NDC item 70860080141

NDC 970860-801
NDC 1070860-801-41
NDC Item70860080141
packaging1 mL in 1 VIAL
ANDAANDA200122
FDA SPL set id353618
LabelerAthenex Pharmaceutical Division, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2020-08-31
Marketing effective time low2017-02-22
Marketing statusCOMPLETED

NDC item 71872708001

NDC 971872-7080
NDC 1071872-7080-1
NDC Item71872708001
packaging1 VIAL in 1 BAG (71872-7080-1) / 1 mL in 1 VIAL
ANDAANDA078630
FDA SPL set id711465
LabelerMedical Purchasing Solutions. LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2009-05-20
Marketing statusACTIVE

NDC item 71872713001

NDC 971872-7130
NDC 1071872-7130-1
NDC Item71872713001
packaging1 VIAL in 1 BAG (71872-7130-1) / 1 mL in 1 VIAL
ANDAANDA200122
FDA SPL set id448756
LabelerMedical Purchasing Solutions, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2017-02-22
Marketing statusACTIVE

NDC item 72843010110

NDC 972843-101
NDC 1072843-101-10
NDC Item72843010110
packaging10 VIAL in 1 BOX (72843-101-10) / 1 mL in 1 VIAL
ANDAANDA200122
FDA SPL set id372809
LabelerUBI Pharma Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2014-12-15
Marketing statusACTIVE