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NDC properties for NDC 9 0703-9503

NDC item 00703950301

NDC 90703-9503
NDC 100703-9503-01
NDC Item00703950301
packaging5 mL in 1 VIAL, SINGLE-DOSE
ANDAANDA073303
LabelerTeva Parenteral Medicines, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low1991-11-01
Marketing statusACTIVE

NDC item 00703950303

NDC 90703-9503
NDC 100703-9503-03
NDC Item00703950303
packaging10 VIAL, SINGLE-DOSE in 1 CARTON (0703-9503-03) / 5 mL in 1 VIAL, SINGLE-DOSE (0703-9503-01)
ANDAANDA073303
LabelerTeva Parenteral Medicines, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low1991-11-01
Marketing statusACTIVE

NDC item 67457077800

NDC 967457-778
NDC 1067457-778-00
NDC Item67457077800
packaging5 mL in 1 VIAL, SINGLE-DOSE
ANDAANDA206607
LabelerMylan Institutional LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2025-10-31
Marketing effective time low2017-12-31
Marketing statusCOMPLETED

NDC item 67457077805

NDC 967457-778
NDC 1067457-778-05
NDC Item67457077805
packaging10 VIAL, SINGLE-DOSE in 1 CARTON (67457-778-05) / 5 mL in 1 VIAL, SINGLE-DOSE (67457-778-00)
ANDAANDA206607
LabelerMylan Institutional LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2025-10-31
Marketing effective time low2017-12-31
Marketing statusCOMPLETED

NDC item 67457092100

NDC 967457-921
NDC 1067457-921-00
NDC Item67457092100
packaging5 mL in 1 VIAL, SINGLE-DOSE
ANDAANDA206607
LabelerMylan Institutional LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2025-03-31
Marketing effective time low2020-10-12
Marketing statusCOMPLETED

NDC item 67457092105

NDC 967457-921
NDC 1067457-921-05
NDC Item67457092105
packaging10 VIAL, SINGLE-DOSE in 1 CARTON (67457-921-05) / 5 mL in 1 VIAL, SINGLE-DOSE (67457-921-00)
ANDAANDA206607
LabelerMylan Institutional LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time high2025-03-31
Marketing effective time low2020-10-12
Marketing statusCOMPLETED

NDC item 70069036101

NDC 970069-361
NDC 1070069-361-01
NDC Item70069036101
packaging5 mL in 1 VIAL
ANDAANDA212231
COLORTEXTYELLOW(Clear, colorless to pale yellow solution)
ColorC48330 __
LabelerSomerset Therapeutics, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2019-08-29
Marketing statusACTIVE

NDC item 70069036110

NDC 970069-361
NDC 1070069-361-10
NDC Item70069036110
packaging10 VIAL in 1 CARTON (70069-361-10) / 5 mL in 1 VIAL (70069-361-01)
ANDAANDA212231
COLORTEXTYELLOW(Clear, colorless to pale yellow solution)
ColorC48330 __
LabelerSomerset Therapeutics, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2019-08-29
Marketing statusACTIVE