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NDC properties for NDC 9 0703-9514

NDC item 00703951401

NDC 90703-9514
NDC 100703-9514-01
NDC Item00703951401
packaging10 mL in 1 VIAL, MULTI-DOSE
ANDAANDA073303
FDA SPL set id716741
FDA SPL set id716880
FDA SPL set id804133
LabelerTeva Parenteral Medicines, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-07-11
Marketing statusACTIVE

NDC item 00703951403

NDC 90703-9514
NDC 100703-9514-03
NDC Item00703951403
packaging10 VIAL, MULTI-DOSE in 1 CARTON (0703-9514-03) / 10 mL in 1 VIAL, MULTI-DOSE (0703-9514-01)
ANDAANDA073303
FDA SPL set id716741
FDA SPL set id716880
FDA SPL set id804133
LabelerTeva Parenteral Medicines, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-07-11
Marketing statusACTIVE

NDC item 00703951481

NDC 90703-9514
NDC 100703-9514-81
NDC Item00703951481
packaging10 mL in 1 VIAL, MULTI-DOSE
ANDAANDA073303
FDA SPL set id716741
FDA SPL set id716880
FDA SPL set id804133
LabelerTeva Parenteral Medicines, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-07-11
Marketing statusACTIVE

NDC item 00703951483

NDC 90703-9514
NDC 100703-9514-83
NDC Item00703951483
packaging10 VIAL, MULTI-DOSE in 1 CARTON (0703-9514-83) / 10 mL in 1 VIAL, MULTI-DOSE (0703-9514-81)
ANDAANDA073303
FDA SPL set id716741
FDA SPL set id716880
FDA SPL set id804133
LabelerTeva Parenteral Medicines, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-07-11
Marketing statusCOMPLETED

NDC item 00703951491

NDC 90703-9514
NDC 100703-9514-91
NDC Item00703951491
packaging10 mL in 1 VIAL, MULTI-DOSE
ANDAANDA073303
FDA SPL set id716741
FDA SPL set id716880
FDA SPL set id804133
LabelerTeva Parenteral Medicines, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-07-11
Marketing statusACTIVE

NDC item 00703951493

NDC 90703-9514
NDC 100703-9514-93
NDC Item00703951493
packaging10 VIAL, MULTI-DOSE in 1 CARTON (0703-9514-93) / 10 mL in 1 VIAL, MULTI-DOSE (0703-9514-91)
ANDAANDA073303
FDA SPL set id716741
FDA SPL set id716880
FDA SPL set id804133
LabelerTeva Parenteral Medicines, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-07-11
Marketing statusACTIVE

NDC item 00703952601

NDC 90703-9526
NDC 100703-9526-01
NDC Item00703952601
packaging1 VIAL, MULTI-DOSE in 1 CARTON (0703-9526-01) / 30 mL in 1 VIAL, MULTI-DOSE
ANDAANDA073303
FDA SPL set id716741
FDA SPL set id804133
LabelerTeva Parenteral Medicines, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-08-15
Marketing statusACTIVE

NDC item 00703952681

NDC 90703-9526
NDC 100703-9526-81
NDC Item00703952681
packaging1 VIAL, MULTI-DOSE in 1 CARTON (0703-9526-81) / 30 mL in 1 VIAL, MULTI-DOSE
ANDAANDA073303
FDA SPL set id716741
FDA SPL set id804133
LabelerTeva Parenteral Medicines, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-08-15
Marketing statusactive

NDC item 67457077930

NDC 967457-779
NDC 1067457-779-30
NDC Item67457077930
packaging1 VIAL, MULTI-DOSE in 1 CARTON (67457-779-30) / 30 mL in 1 VIAL, MULTI-DOSE
ANDAANDA206607
FDA SPL set id788139
LabelerMylan Institutional LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2017-12-31
Marketing statusACTIVE

NDC item 67457092230

NDC 967457-922
NDC 1067457-922-30
NDC Item67457092230
packaging1 VIAL, MULTI-DOSE in 1 CARTON (67457-922-30) / 30 mL in 1 VIAL, MULTI-DOSE
ANDAANDA206607
FDA SPL set id804325
LabelerMylan Institutional LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2025-03-31
Marketing effective time low2020-10-12
Marketing statusACTIVE

NDC item 70069036201

NDC 970069-362
NDC 1070069-362-01
NDC Item70069036201
packaging10 mL in 1 VIAL
ANDAANDA212231
COLORTEXTYELLOW(Clear, colorless to pale yellow solution)
ColorC48330 __
FDA SPL set id723076
LabelerSomerset Therapeutics, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2019-08-29
Marketing statusACTIVE

NDC item 70069036210

NDC 970069-362
NDC 1070069-362-10
NDC Item70069036210
packaging10 VIAL in 1 CARTON (70069-362-10) / 10 mL in 1 VIAL (70069-362-01)
ANDAANDA212231
COLORTEXTYELLOW(Clear, colorless to pale yellow solution)
ColorC48330 __
FDA SPL set id723076
LabelerSomerset Therapeutics, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2019-08-29
Marketing statusACTIVE

NDC item 70069036301

NDC 970069-363
NDC 1070069-363-01
NDC Item70069036301
packaging1 VIAL in 1 CARTON (70069-363-01) / 30 mL in 1 VIAL
ANDAANDA212231
COLORTEXTYELLOW(Clear, colorless to pale yellow solution)
ColorC48330 __
FDA SPL set id723076
LabelerSomerset Therapeutics, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2019-08-29
Marketing statusACTIVE