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NDC properties for NDC 9 0641-6118

NDC item 00641611801

NDC 90641-6118
NDC 100641-6118-01
NDC Item00641611801
packaging100 mL in 1 VIAL, PHARMACY BULK PACKAGE (0641-6118-01)
ANDAANDA065403
FDA SPL set id802596
LabelerHikma Pharmaceuticals USA Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2009-12-03
Marketing statusACTIVE

NDC item 00641612101

NDC 90641-6121
NDC 100641-6121-01
NDC Item00641612101
packaging100 mL in 1 VIAL, PHARMACY BULK PACKAGE (0641-6121-01)
ANDAANDA065403
FDA SPL set id218755
LabelerWest-Ward Pharmaceuticals Corp.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2009-12-03
Marketing statusACTIVE

NDC item 00781303446

NDC 90781-3034
NDC 100781-3034-46
NDC Item00781303446
packaging1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PHARMACY BULK PACKAGE (0781-3034-46)
ANDAANDA065240
FDA SPL set id526354
LabelerSandoz Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2014-06-30
Marketing effective time low2006-07-25
Marketing statusCOMPLETED

NDC item 25021014499

NDC 925021-144
NDC 1025021-144-99
NDC Item25021014499
packaging1 BOTTLE in 1 CARTON (25021-144-99) / 100 mL in 1 BOTTLE
ANDAANDA065403
FDA SPL set id537054
LabelerSagent Pharmaceuticals
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2010-08-12
Marketing statusACTIVE

NDC item 25021018899

NDC 925021-188
NDC 1025021-188-99
NDC Item25021018899
packaging1 BOTTLE in 1 CARTON (25021-188-99) / 100 mL in 1 BOTTLE
ANDAANDA090578
FDA SPL set id549274
LabelerSagent Pharmaceuticals
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2021-03-31
Marketing effective time low2017-08-15
Marketing statusCOMPLETED

NDC item 44567021201

NDC 944567-212
NDC 1044567-212-01
NDC Item44567021201
packaging1 VIAL in 1 CARTON (44567-212-01) / 100 mL in 1 VIAL
ANDAANDA065188
FDA SPL set id802523
LabelerWG Critical Care, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2005-11-25
Marketing statusACTIVE

NDC item 55150011801

NDC 955150-118
NDC 1055150-118-01
NDC Item55150011801
packaging1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (55150-118-01) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE
ANDAANDA090339
COLORTEXTWHITE(White to Off-white)
ColorC48325 __
FDA SPL set id705808
FDA SPL set id790102
LabelerEugia US LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2012-02-10
Marketing statusACTIVE

NDC item 55150011899

NDC 955150-118
NDC 1055150-118-99
NDC Item55150011899
packaging1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (55150-118-99) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE
ANDAANDA090339
COLORTEXTWHITE(White to Off-white)
ColorC48325 __
FDA SPL set id705808
FDA SPL set id790102
LabelerEugia US LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2012-02-10
Marketing statusACTIVE

NDC item 63323037062

NDC 963323-370
NDC 1063323-370-62
NDC Item63323037062
packaging10 VIAL in 1 CARTON (63323-370-62) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
ANDAANDA065314
FDA SPL set id440211
LabelerFresenius Kabi USA, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2016-07-25
Marketing effective time low2006-11-27
Marketing statusCOMPLETED

NDC item 66794020815

NDC 966794-208
NDC 1066794-208-15
NDC Item66794020815
packaging1 BOTTLE in 1 CARTON (66794-208-15) / 100 mL in 1 BOTTLE
ANDAANDA090578
FDA SPL set id683048
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 66794024315

NDC 966794-243
NDC 1066794-243-15
NDC Item66794024315
packaging1 BOTTLE in 1 CARTON (66794-243-15) / 100 mL in 1 BOTTLE
ANDAANDA090578
FDA SPL set id695618
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 67457064910

NDC 967457-649
NDC 1067457-649-10
NDC Item67457064910
packaging1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (67457-649-10) / 92 mL in 1 VIAL, PHARMACY BULK PACKAGE
ANDAANDA202197
FDA SPL set id675550
LabelerMylan Institutional LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2023-12-31
Marketing effective time low2014-04-08
Marketing statusCOMPLETED

NDC item 70594008301

NDC 970594-083
NDC 1070594-083-01
NDC Item70594008301
packaging1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (70594-083-01) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE
ANDAANDA090578
FDA SPL set id685160
LabelerXellia Pharmaceuticals USA LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2021-01-10
Marketing statusACTIVE

NDC item 71288000775

NDC 971288-007
NDC 1071288-007-75
NDC Item71288000775
packaging1 BOTTLE in 1 CARTON (71288-007-75) / 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE
ANDAANDA090578
FDA SPL set id770217
LabelerMeitheal Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2024-07-31
Marketing effective time low2018-12-17
Marketing statusCOMPLETED

NDC item 71288003375

NDC 971288-033
NDC 1071288-033-75
NDC Item71288003375
packaging1 BOTTLE in 1 CARTON (71288-033-75) / 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE
ANDAANDA065314
FDA SPL set id712327
FDA SPL set id787683
LabelerMeitheal Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2006-11-27
Marketing statusACTIVE

NDC item 71288003391

NDC 971288-033
NDC 1071288-033-91
NDC Item71288003391
packaging1 BOTTLE in 1 CARTON (71288-033-91) / 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE
ANDAANDA065314
FDA SPL set id712327
FDA SPL set id787683
LabelerMeitheal Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2006-11-27
Marketing statusACTIVE

NDC item 72603044401

NDC 972603-444
NDC 1072603-444-01
NDC Item72603044401
packaging10 BOTTLE in 1 CARTON (72603-444-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE
ANDAANDA065314
FDA SPL set id793826
LabelerNorthStar Rx, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-03-01
Marketing statusactive