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NDC properties for NDC 9 0574-4031

NDC item 00574403105

NDC 90574-4031
NDC 100574-4031-05
NDC Item00574403105
packaging5 mL in 1 BOTTLE, PLASTIC (0574-4031-05)
ANDAANDA212715
FDA SPL set id777631
LabelerPadagis US LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-03-17
Marketing statusACTIVE

NDC item 00574403110

NDC 90574-4031
NDC 100574-4031-10
NDC Item00574403110
packaging10 mL in 1 BOTTLE, PLASTIC (0574-4031-10)
ANDAANDA212715
FDA SPL set id777631
LabelerPadagis US LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-03-17
Marketing statusACTIVE

NDC item 00574403125

NDC 90574-4031
NDC 100574-4031-25
NDC Item00574403125
packaging2.5 mL in 1 BOTTLE, PLASTIC (0574-4031-25)
ANDAANDA212715
FDA SPL set id777631
LabelerPadagis US LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-03-17
Marketing statusACTIVE

NDC item 24208029505

NDC 924208-295
NDC 1024208-295-05
NDC Item24208029505
packaging1 BOTTLE, DROPPER in 1 CARTON (24208-295-05) / 5 mL in 1 BOTTLE, DROPPER
ANDAANDA064134
FDA SPL set id736214
LabelerBausch & Lomb Incorporated
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low1999-10-27
Marketing statusACTIVE

NDC item 24208029510

NDC 924208-295
NDC 1024208-295-10
NDC Item24208029510
packaging1 BOTTLE, DROPPER in 1 CARTON (24208-295-10) / 10 mL in 1 BOTTLE, DROPPER
ANDAANDA064134
FDA SPL set id736214
LabelerBausch & Lomb Incorporated
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low1999-10-27
Marketing statusACTIVE

NDC item 24208029525

NDC 924208-295
NDC 1024208-295-25
NDC Item24208029525
packaging1 BOTTLE, DROPPER in 1 CARTON (24208-295-25) / 2.5 mL in 1 BOTTLE, DROPPER
ANDAANDA064134
FDA SPL set id736214
LabelerBausch & Lomb Incorporated
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low1999-10-27
Marketing statusACTIVE

NDC item 50090113500

NDC 950090-1135
NDC 1050090-1135-0
NDC Item50090113500
packaging2.5 mL in 1 BOTTLE (50090-1135-0)
FDA SPL set id718677
LabelerA-S Medication Solutions
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2009-01-02
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA050592

NDC item 50090113600

NDC 950090-1136
NDC 1050090-1136-0
NDC Item50090113600
packaging5 mL in 1 BOTTLE (50090-1136-0)
FDA SPL set id803024
LabelerA-S Medication Solutions
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2009-01-02
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA050592

NDC item 50090189300

NDC 950090-1893
NDC 1050090-1893-0
NDC Item50090189300
packaging1 BOTTLE, DROPPER in 1 CARTON (50090-1893-0) / 5 mL in 1 BOTTLE, DROPPER
ANDAANDA064134
FDA SPL set id771442
LabelerA-S Medication Solutions
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low1999-10-27
Marketing statusACTIVE

NDC item 50090191400

NDC 950090-1914
NDC 1050090-1914-0
NDC Item50090191400
packaging1 BOTTLE, DROPPER in 1 CARTON (50090-1914-0) / 2.5 mL in 1 BOTTLE, DROPPER
ANDAANDA064134
FDA SPL set id693387
LabelerA-S Medication Solutions
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low1999-10-27
Marketing statusACTIVE

NDC item 50090726700

NDC 950090-7267
NDC 1050090-7267-0
NDC Item50090726700
packaging5 mL in 1 BOTTLE, PLASTIC (50090-7267-0)
ANDAANDA212715
FDA SPL set id817223
LabelerA-S Medication Solutions
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-03-17
Marketing statusACTIVE

NDC item 52959098401

NDC 952959-984
NDC 1052959-984-01
NDC Item52959098401
FDA SPL set id57994
LabelerH.J. Harkins Company, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2009-01-02
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA050592

NDC item 52959098410

NDC 952959-984
NDC 1052959-984-10
NDC Item52959098410
packaging10 mL in 1 BOTTLE (52959-984-10)
FDA SPL set id57994
LabelerH.J. Harkins Company, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2009-01-02
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA050592

NDC item 55700091505

NDC 955700-915
NDC 1055700-915-05
NDC Item55700091505
packaging1 BOTTLE, DROPPER in 1 CARTON (55700-915-05) / 5 mL in 1 BOTTLE, DROPPER
ANDAANDA064134
FDA SPL set id653524
LabelerQuality Care Products, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2021-07-08
Marketing statusACTIVE

NDC item 61314064705

NDC 961314-647
NDC 1061314-647-05
NDC Item61314064705
packaging5 mL in 1 BOTTLE (61314-647-05)
FDA SPL set id871293
LabelerSandoz Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2009-01-02
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA050592

NDC item 61314064710

NDC 961314-647
NDC 1061314-647-10
NDC Item61314064710
packaging10 mL in 1 BOTTLE (61314-647-10)
FDA SPL set id871293
LabelerSandoz Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2009-01-02
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA050592

NDC item 61314064725

NDC 961314-647
NDC 1061314-647-25
NDC Item61314064725
packaging2.5 mL in 1 BOTTLE (61314-647-25)
FDA SPL set id871293
LabelerSandoz Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2009-01-02
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA050592

NDC item 63629957001

NDC 963629-9570
NDC 1063629-9570-1
NDC Item63629957001
packaging2.5 mL in 1 BOTTLE, PLASTIC (63629-9570-1)
ANDAANDA212715
FDA SPL set id763323
LabelerBryant Ranch Prepack
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-03-17
Marketing statusACTIVE

NDC item 63629957101

NDC 963629-9571
NDC 1063629-9571-1
NDC Item63629957101
packaging5 mL in 1 BOTTLE, PLASTIC (63629-9571-1)
ANDAANDA212715
FDA SPL set id763569
LabelerBryant Ranch Prepack
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-03-17
Marketing statusACTIVE

NDC item 63629957201

NDC 963629-9572
NDC 1063629-9572-1
NDC Item63629957201
packaging10 mL in 1 BOTTLE, PLASTIC (63629-9572-1)
ANDAANDA212715
FDA SPL set id763269
LabelerBryant Ranch Prepack
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-03-17
Marketing statusACTIVE

NDC item 67296066501

NDC 967296-0665
NDC 1067296-0665-1
NDC Item67296066501
packaging5 mL in 1 BOTTLE (67296-0665-1)
FDA SPL set id813479
LabelerRedpharm Drug
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2009-01-02
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA050592

NDC item 68071182102

NDC 968071-1821
NDC 1068071-1821-2
NDC Item68071182102
packaging1 BOTTLE, DROPPER in 1 CARTON (68071-1821-2) / 2.5 mL in 1 BOTTLE, DROPPER
ANDAANDA064134
FDA SPL set id858986
LabelerNuCare Pharmaceuticals,Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low1999-10-27
Marketing statusACTIVE

NDC item 68071420305

NDC 968071-4203
NDC 1068071-4203-5
NDC Item68071420305
packaging5 mL in 1 BOX (68071-4203-5)
ANDAANDA064134
FDA SPL set id790175
LabelerNuCare Pharmaceuticals,Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low1999-10-27
Marketing statusACTIVE

NDC item 69238137302

NDC 969238-1373
NDC 1069238-1373-2
NDC Item69238137302
packaging1 BOTTLE, PLASTIC in 1 CARTON (69238-1373-2) / 2.5 mL in 1 BOTTLE, PLASTIC
ANDAANDA212991
COLORTEXTwhite(white to off-white uniform suspension)
ColorC48325 __
FDA SPL set id803363
LabelerAmneal Pharmaceuticals NY LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2021-07-17
Marketing statusACTIVE

NDC item 69238137403

NDC 969238-1374
NDC 1069238-1374-3
NDC Item69238137403
packaging1 BOTTLE, PLASTIC in 1 CARTON (69238-1374-3) / 5 mL in 1 BOTTLE, PLASTIC
ANDAANDA212991
COLORTEXTwhite(white to off-white uniform suspension)
ColorC48325 __
FDA SPL set id803363
LabelerAmneal Pharmaceuticals NY LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2021-07-17
Marketing statusACTIVE

NDC item 69238137506

NDC 969238-1375
NDC 1069238-1375-6
NDC Item69238137506
packaging1 BOTTLE, PLASTIC in 1 CARTON (69238-1375-6) / 10 mL in 1 BOTTLE, PLASTIC
ANDAANDA212991
COLORTEXTwhite(white to off-white uniform suspension)
ColorC48325 __
FDA SPL set id803363
LabelerAmneal Pharmaceuticals NY LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2021-07-17
Marketing statusACTIVE

NDC item 70518399400

NDC 970518-3994
NDC 1070518-3994-0
NDC Item70518399400
packaging5 mL in 1 BOTTLE (70518-3994-0)
FDA SPL set id766955
LabelerREMEDYREPACK INC.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2024-01-24
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA050592

NDC item 72162112802

NDC 972162-1128
NDC 1072162-1128-2
NDC Item72162112802
packaging10 mL in 1 BOTTLE, PLASTIC (72162-1128-2)
ANDAANDA212715
FDA SPL set id847199
LabelerBryant Ranch Prepack
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-03-17
Marketing statusACTIVE

NDC item 72162112804

NDC 972162-1128
NDC 1072162-1128-4
NDC Item72162112804
packaging5 mL in 1 BOTTLE, PLASTIC (72162-1128-4)
ANDAANDA212715
FDA SPL set id847199
LabelerBryant Ranch Prepack
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-03-17
Marketing statusACTIVE

NDC item 72162112807

NDC 972162-1128
NDC 1072162-1128-7
NDC Item72162112807
packaging2.5 mL in 1 BOTTLE, PLASTIC (72162-1128-7)
ANDAANDA212715
FDA SPL set id847199
LabelerBryant Ranch Prepack
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-03-17
Marketing statusACTIVE

NDC item 80425026001

NDC 980425-0260
NDC 1080425-0260-1
NDC Item80425026001
packaging5 mL in 1 BOTTLE, PLASTIC (80425-0260-1)
ANDAANDA212715
FDA SPL set id848958
LabelerAdvanced Rx Pharmacy of Tennessee, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2023-02-15
Marketing statusACTIVE

NDC item 80425036601

NDC 980425-0366
NDC 1080425-0366-1
NDC Item80425036601
packaging5 mL in 1 BOTTLE (80425-0366-1)
FDA SPL set id847557
LabelerAdvanced Rx of Tennessee, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2023-11-02
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA050592