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HomeSearchNDC id 1659598

NDC properties for NDC 9 0409-2987

NDC item 00409298703

NDC 90409-2987
NDC 100409-2987-03
NDC Item00409298703
packaging10 VIAL in 1 TRAY (0409-2987-03) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0409-2987-23)
ANDAANDA065310
FDA SPL set id687293
LabelerHospira, Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2006-07-25
Marketing statusACTIVE

NDC item 00409298723

NDC 90409-2987
NDC 100409-2987-23
NDC Item00409298723
packaging1 in 1 VIAL
ANDAANDA065241
FDA SPL set id687293
LabelerHospira, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2013-10-01
Marketing effective time low2006-07-25
Marketing statusCOMPLETED

NDC item 00409298749

NDC 90409-2987
NDC 100409-2987-49
NDC Item00409298749
ANDAANDA065241
FDA SPL set id687293
LabelerHospira, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2013-10-01
Marketing effective time low2006-07-25
Marketing statusCOMPLETED

NDC item 00641611701

NDC 90641-6117
NDC 100641-6117-01
NDC Item00641611701
packaging3 g in 1 VIAL
ANDAANDA065406
FDA SPL set id802642
LabelerHikma Pharmaceuticals USA Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2009-12-22
Marketing statusACTIVE

NDC item 00641611710

NDC 90641-6117
NDC 100641-6117-10
NDC Item00641611710
packaging10 VIAL in 1 CARTON (0641-6117-10) / 3 g in 1 VIAL (0641-6117-01)
ANDAANDA065406
FDA SPL set id802642
LabelerHikma Pharmaceuticals USA Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2009-12-22
Marketing statusACTIVE

NDC item 00641612001

NDC 90641-6120
NDC 100641-6120-01
NDC Item00641612001
packaging3 g in 1 VIAL
ANDAANDA065406
FDA SPL set id440588
LabelerHikma Pharmaceuticals USA Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2009-12-22
Marketing statusACTIVE

NDC item 00641612010

NDC 90641-6120
NDC 100641-6120-10
NDC Item00641612010
packaging10 VIAL in 1 CARTON (0641-6120-10) / 3 g in 1 VIAL (0641-6120-01)
ANDAANDA065406
FDA SPL set id440588
LabelerHikma Pharmaceuticals USA Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2009-12-22
Marketing statusACTIVE

NDC item 00641612301

NDC 90641-6123
NDC 100641-6123-01
NDC Item00641612301
packaging8 mL in 1 VIAL
ANDAANDA065406
FDA SPL set id440293
LabelerHikma Pharmaceuticals USA Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2009-12-22
Marketing statusACTIVE

NDC item 00641612310

NDC 90641-6123
NDC 100641-6123-10
NDC Item00641612310
packaging10 VIAL in 1 CARTON (0641-6123-10) / 8 mL in 1 VIAL (0641-6123-01)
ANDAANDA065406
FDA SPL set id440293
LabelerHikma Pharmaceuticals USA Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2009-12-22
Marketing statusACTIVE

NDC item 00781303370

NDC 90781-3033
NDC 100781-3033-70
NDC Item00781303370
packaging1 in 1 VIAL
ANDAANDA065241
FDA SPL set id526593
LabelerSandoz Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2020-05-31
Marketing effective time low2006-07-25
Marketing statusCOMPLETED

NDC item 00781303395

NDC 90781-3033
NDC 100781-3033-95
NDC Item00781303395
packaging10 VIAL in 1 CARTON (0781-3033-95) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0781-3033-70)
ANDAANDA065241
FDA SPL set id526593
LabelerSandoz Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2020-05-31
Marketing effective time low2006-07-25
Marketing statusCOMPLETED

NDC item 25021014330

NDC 925021-143
NDC 1025021-143-30
NDC Item25021014330
packaging10 VIAL in 1 CARTON (25021-143-30) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
ANDAANDA065406
FDA SPL set id612973
LabelerSagent Pharmaceuticals
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2010-06-30
Marketing statusACTIVE

NDC item 25021018730

NDC 925021-187
NDC 1025021-187-30
NDC Item25021018730
packaging10 VIAL in 1 CARTON (25021-187-30) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
ANDAANDA090579
FDA SPL set id549185
LabelerSagent Pharmaceuticals
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2021-03-31
Marketing effective time low2017-08-15
Marketing statusCOMPLETED

NDC item 44567015010

NDC 944567-150
NDC 1044567-150-10
NDC Item44567015010
packaging10 VIAL in 1 CARTON (44567-150-10) / 20 mL in 1 VIAL
ANDAANDA201406
FDA SPL set id805335
LabelerWG Critical Care, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2021-11-30
Marketing statusACTIVE

NDC item 44567021110

NDC 944567-211
NDC 1044567-211-10
NDC Item44567021110
packaging10 VIAL in 1 CARTON (44567-211-10) / 20 mL in 1 VIAL
ANDAANDA065176
FDA SPL set id803837
LabelerWG Critical Care, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2005-11-30
Marketing statusACTIVE

NDC item 55150011701

NDC 955150-117
NDC 1055150-117-01
NDC Item55150011701
ANDAANDA090349
COLORTEXTWHITE(White to Off-white)
ColorC48325 __
FDA SPL set id705782
FDA SPL set id790857
LabelerEugia US LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2012-02-10
Marketing statusACTIVE

NDC item 55150011710

NDC 955150-117
NDC 1055150-117-10
NDC Item55150011710
packaging10 VIAL in 1 CARTON (55150-117-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
ANDAANDA090349
COLORTEXTWHITE(White to Off-white)
ColorC48325 __
FDA SPL set id705782
FDA SPL set id790857
LabelerEugia US LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2012-02-10
Marketing statusACTIVE

NDC item 55150011720

NDC 955150-117
NDC 1055150-117-20
NDC Item55150011720
packaging10 VIAL in 1 CARTON (55150-117-20) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
ANDAANDA090349
COLORTEXTWHITE(White to Off-white)
ColorC48325 __
FDA SPL set id705782
FDA SPL set id790857
LabelerEugia US LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2012-02-10
Marketing statusACTIVE

NDC item 55150017999

NDC 955150-179
NDC 1055150-179-99
NDC Item55150017999
packaging10 BOTTLE in 1 BOX (55150-179-99) / 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE
ANDAANDA090340
COLORTEXTWHITE(White to Off-white)
ColorC48325 __
FDA SPL set id790857
LabelerEugia US LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2012-09-13
Marketing statusACTIVE

NDC item 63323036920

NDC 963323-369
NDC 1063323-369-20
NDC Item63323036920
packaging10 VIAL in 1 CARTON (63323-369-20) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
ANDAANDA065222
FDA SPL set id460623
LabelerFresenius Kabi USA, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2016-05-05
Marketing effective time low2005-11-29
Marketing statusCOMPLETED

NDC item 66794020702

NDC 966794-207
NDC 1066794-207-02
NDC Item66794020702
packaging1 in 1 VIAL
ANDAANDA090579
FDA SPL set id683064
LabelerPiramal Critical Care Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2023-05-15
Marketing effective time low2019-05-20
Marketing statusCOMPLETED

NDC item 66794020741

NDC 966794-207
NDC 1066794-207-41
NDC Item66794020741
packaging10 VIAL in 1 CARTON (66794-207-41) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (66794-207-02)
ANDAANDA090579
FDA SPL set id683064
LabelerPiramal Critical Care Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2023-05-15
Marketing effective time low2019-05-20
Marketing statusCOMPLETED

NDC item 66794024202

NDC 966794-242
NDC 1066794-242-02
NDC Item66794024202
packaging1 in 1 VIAL
ANDAANDA090579
FDA SPL set id695619
LabelerPiramal Critical Care Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2023-05-15
Marketing effective time low2023-01-01
Marketing statusCOMPLETED

NDC item 66794024241

NDC 966794-242
NDC 1066794-242-41
NDC Item66794024241
packaging10 VIAL in 1 CARTON (66794-242-41) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (66794-242-02)
ANDAANDA090579
FDA SPL set id695619
LabelerPiramal Critical Care Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2023-05-15
Marketing effective time low2023-01-01
Marketing statusCOMPLETED

NDC item 67457022600

NDC 967457-226
NDC 1067457-226-00
NDC Item67457022600
ANDAANDA065316
LabelerMylan Institutional LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2014-05-31
Marketing effective time low2012-11-27
Marketing statusCOMPLETED

NDC item 67457034903

NDC 967457-349
NDC 1067457-349-03
NDC Item67457034903
packaging1 VIAL in 1 CARTON (67457-349-03) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
ANDAANDA201024
FDA SPL set id675125
LabelerMylan Institutional LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2024-02-29
Marketing effective time low2014-04-08
Marketing statusCOMPLETED

NDC item 67457034910

NDC 967457-349
NDC 1067457-349-10
NDC Item67457034910
packaging10 VIAL in 1 CARTON (67457-349-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
ANDAANDA201024
FDA SPL set id675125
LabelerMylan Institutional LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2024-02-29
Marketing effective time low2014-04-08
Marketing statusCOMPLETED

NDC item 67850013100

NDC 967850-131
NDC 1067850-131-00
NDC Item67850013100
packaging1 in 1 VIAL, GLASS
ANDAANDA201406
FDA SPL set id770928
LabelerMethapharm, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-01-01
Marketing statusACTIVE

NDC item 67850013110

NDC 967850-131
NDC 1067850-131-10
NDC Item67850013110
packaging10 VIAL, GLASS in 1 CARTON (67850-131-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (67850-131-00)
ANDAANDA201406
FDA SPL set id770928
LabelerMethapharm, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-01-01
Marketing statusACTIVE

NDC item 70594008201

NDC 970594-082
NDC 1070594-082-01
NDC Item70594008201
packaging1 in 1 VIAL
ANDAANDA090579
FDA SPL set id687752
LabelerXellia Pharmaceuticals USA LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2021-01-10
Marketing statusACTIVE

NDC item 70594008202

NDC 970594-082
NDC 1070594-082-02
NDC Item70594008202
packaging10 VIAL in 1 CARTON (70594-082-02) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (70594-082-01)
ANDAANDA090579
FDA SPL set id687752
LabelerXellia Pharmaceuticals USA LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2021-01-10
Marketing statusACTIVE

NDC item 71288000630

NDC 971288-006
NDC 1071288-006-30
NDC Item71288000630
packaging10 VIAL, SINGLE-DOSE in 1 CARTON (71288-006-30) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (71288-006-31)
ANDAANDA090579
FDA SPL set id770198
LabelerMeitheal Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2024-11-30
Marketing effective time low2022-01-17
Marketing statusCOMPLETED

NDC item 71288000631

NDC 971288-006
NDC 1071288-006-31
NDC Item71288000631
packaging1 in 1 VIAL, SINGLE-DOSE
ANDAANDA090579
FDA SPL set id770198
LabelerMeitheal Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2024-11-30
Marketing effective time low2022-01-17
Marketing statusCOMPLETED

NDC item 71288003220

NDC 971288-032
NDC 1071288-032-20
NDC Item71288003220
packaging1 in 1 VIAL, SINGLE-DOSE
ANDAANDA065222
FDA SPL set id749843
FDA SPL set id787470
LabelerMeitheal Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2005-11-29
Marketing statusACTIVE

NDC item 71288003221

NDC 971288-032
NDC 1071288-032-21
NDC Item71288003221
packaging10 VIAL, SINGLE-DOSE in 1 CARTON (71288-032-21) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (71288-032-20)
ANDAANDA065222
FDA SPL set id749843
FDA SPL set id787470
LabelerMeitheal Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2005-11-29
Marketing statusACTIVE

NDC item 71288003291

NDC 971288-032
NDC 1071288-032-91
NDC Item71288003291
packaging1 in 1 VIAL, SINGLE-DOSE
ANDAANDA065222
FDA SPL set id749843
FDA SPL set id787470
LabelerMeitheal Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2005-11-29
Marketing statusACTIVE

NDC item 71288003292

NDC 971288-032
NDC 1071288-032-92
NDC Item71288003292
packaging10 VIAL, SINGLE-DOSE in 1 CARTON (71288-032-92) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (71288-032-91)
ANDAANDA065222
FDA SPL set id749843
FDA SPL set id787470
LabelerMeitheal Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2005-11-29
Marketing statusACTIVE

NDC item 72485041701

NDC 972485-417
NDC 1072485-417-01
NDC Item72485041701
packaging1 in 1 VIAL
ANDAANDA201024
COLORTEXTwhite(off-white)
ColorC48325 __
FDA SPL set id720326
LabelerArmas Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2023-04-25
Marketing statusACTIVE

NDC item 72485041710

NDC 972485-417
NDC 1072485-417-10
NDC Item72485041710
packaging10 VIAL in 1 CARTON (72485-417-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (72485-417-01)
ANDAANDA201024
COLORTEXTwhite(off-white)
ColorC48325 __
FDA SPL set id720326
LabelerArmas Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2023-04-25
Marketing statusACTIVE

NDC item 72572002201

NDC 972572-022
NDC 1072572-022-01
NDC Item72572002201
packaging1 in 1 VIAL, SINGLE-DOSE
ANDAANDA090579
FDA SPL set id679256
LabelerCivica, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2024-03-11
Marketing effective time low2022-01-10
Marketing statusCOMPLETED

NDC item 72572002210

NDC 972572-022
NDC 1072572-022-10
NDC Item72572002210
packaging10 VIAL, SINGLE-DOSE in 1 CARTON (72572-022-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (72572-022-01)
ANDAANDA090579
FDA SPL set id679256
LabelerCivica, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2024-03-11
Marketing effective time low2022-01-10
Marketing statusCOMPLETED

NDC item 72603033501

NDC 972603-335
NDC 1072603-335-01
NDC Item72603033501
packaging1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (72603-335-01)
ANDAANDA065222
FDA SPL set id793796
LabelerNorthStar Rx, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-03-01
Marketing statusactive

NDC item 72603033510

NDC 972603-335
NDC 1072603-335-10
NDC Item72603033510
packaging10 VIAL, SINGLE-DOSE in 1 CARTON (72603-335-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (72603-335-01)
ANDAANDA065222
FDA SPL set id793796
LabelerNorthStar Rx, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-03-01
Marketing statusACTIVE

NDC item 82449051401

NDC 982449-514
NDC 1082449-514-01
NDC Item82449051401
packaging1 VIAL in 1 CARTON (82449-514-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
ANDAANDA201024
FDA SPL set id803546
LabelerSteriscience Specialties Private Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2023-04-14
Marketing statusACTIVE

NDC item 82449051402

NDC 982449-514
NDC 1082449-514-02
NDC Item82449051402
packaging10 VIAL in 1 CARTON (82449-514-02) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
ANDAANDA201024
FDA SPL set id803546
LabelerSteriscience Specialties Private Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2023-04-14
Marketing statusACTIVE