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HomeSearchNDC id 1597129

NDC properties for NDC 9 0591-3217

NDC item 00591321726

NDC 90591-3217
NDC 100591-3217-26
NDC Item00591321726
packaging5 g in 1 PACKET
ANDAANDA076737
DCSACIII
FDA SPL set id701373
LabelerActavis Pharma, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2015-12-04
Marketing statusACTIVE

NDC item 00591321730

NDC 90591-3217
NDC 100591-3217-30
NDC Item00591321730
packaging30 PACKET in 1 CARTON (0591-3217-30) / 5 g in 1 PACKET (0591-3217-26)
ANDAANDA076737
DCSACIII
FDA SPL set id701373
LabelerActavis Pharma, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2015-12-04
Marketing statusACTIVE

NDC item 00591352426

NDC 90591-3524
NDC 100591-3524-26
NDC Item00591352426
packaging5 g in 1 TUBE
ANDAANDA091073
DCSACIII
FDA SPL set id738425
LabelerActavis Pharma, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2017-10-12
Marketing statusACTIVE

NDC item 00591352430

NDC 90591-3524
NDC 100591-3524-30
NDC Item00591352430
packaging30 TUBE in 1 CARTON (0591-3524-30) / 5 g in 1 TUBE (0591-3524-26)
ANDAANDA091073
DCSACIII
FDA SPL set id738425
LabelerActavis Pharma, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2017-10-12
Marketing statusACTIVE

NDC item 00832112005

NDC 90832-1120
NDC 100832-1120-05
NDC Item00832112005
packaging30 TUBE in 1 CARTON (0832-1120-05) / 5 g in 1 TUBE (0832-1120-65)
COLORTEXTWHITE(clear, transluscent)
ColorC48325 __
DCSACIII
FDA SPL set id710489
LabelerUpsher-Smith Laboratories, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2014-06-16
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA204399

NDC item 00832112035

NDC 90832-1120
NDC 100832-1120-35
NDC Item00832112035
packaging30 PACKET in 1 CARTON (0832-1120-35) / 5 g in 1 PACKET (0832-1120-89)
COLORTEXTWHITE(clear, transluscent)
ColorC48325 __
DCSACIII
FDA SPL set id710489
LabelerUpsher-Smith Laboratories, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2014-06-16
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA204399

NDC item 00832112065

NDC 90832-1120
NDC 100832-1120-65
NDC Item00832112065
packaging5 g in 1 TUBE
COLORTEXTWHITE(clear, transluscent)
ColorC48325 __
DCSACIII
FDA SPL set id710489
LabelerUpsher-Smith Laboratories, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2014-06-16
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA204399

NDC item 00832112089

NDC 90832-1120
NDC 100832-1120-89
NDC Item00832112089
packaging5 g in 1 PACKET
COLORTEXTWHITE(clear, transluscent)
ColorC48325 __
DCSACIII
FDA SPL set id710489
LabelerUpsher-Smith Laboratories, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2014-06-16
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA204399

NDC item 21922001902

NDC 921922-019
NDC 1021922-019-02
NDC Item21922001902
packaging30 PACKET in 1 CARTON (21922-019-02) / 5 g in 1 PACKET
ANDAANDA212984
DCSACIII
FDA SPL set id770936
LabelerEncube Ethicals Private Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-02-14
Marketing statusACTIVE

NDC item 49884051063

NDC 949884-510
NDC 1049884-510-63
NDC Item49884051063
packaging5 g in 1 PACKET
ANDAANDA076744
DCSACIII
FDA SPL set id660010
LabelerPar Pharmaceutical, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2015-09-02
Marketing statusACTIVE

NDC item 49884051072

NDC 949884-510
NDC 1049884-510-72
NDC Item49884051072
packaging30 PACKET in 1 CARTON (49884-510-72) / 5 g in 1 PACKET (49884-510-63)
ANDAANDA076744
DCSACIII
FDA SPL set id660010
LabelerPar Pharmaceutical, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2015-09-02
Marketing statusACTIVE

NDC item 63629212501

NDC 963629-2125
NDC 1063629-2125-1
NDC Item63629212501
packaging30 PACKET in 1 CARTON (63629-2125-1) / 5 g in 1 PACKET
ANDAANDA076744
DCSACIII
FDA SPL set id762728
LabelerBryant Ranch Prepack
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2015-09-02
Marketing statusACTIVE

NDC item 63629958501

NDC 963629-9585
NDC 1063629-9585-1
NDC Item63629958501
packaging30 PACKET in 1 CARTON (63629-9585-1) / 5 g in 1 PACKET
ANDAANDA212984
DCSACIII
FDA SPL set id785842
LabelerBryant Ranch Prepack
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2021-11-19
Marketing statusACTIVE

NDC item 64380015201

NDC 964380-152
NDC 1064380-152-01
NDC Item64380015201
packaging5 g in 1 DOSE PACK
ANDAANDA076744
COLORTEXTWHITE(clear, colorless)
ColorC48325 __
DCSACIII
FDA SPL set id793741
LabelerStrides Pharma Science Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-06-27
Marketing statusACTIVE

NDC item 64380015202

NDC 964380-152
NDC 1064380-152-02
NDC Item64380015202
packaging30 DOSE PACK in 1 CARTON (64380-152-02) / 5 g in 1 DOSE PACK
ANDAANDA076744
COLORTEXTWHITE(clear, colorless)
ColorC48325 __
DCSACIII
FDA SPL set id793741
LabelerStrides Pharma Science Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-06-27
Marketing statusACTIVE

NDC item 66993093430

NDC 966993-934
NDC 1066993-934-30
NDC Item66993093430
packaging30 TUBE in 1 CARTON (66993-934-30) / 5 g in 1 TUBE (66993-934-54)
DCSACIII
FDA SPL set id304583
LabelerPrasco Laboratories
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time high2019-02-12
Marketing effective time low2014-06-09
Marketing statusCOMPLETED
NDA_AUTHORIZED_GENERICNDA021454

NDC item 66993093454

NDC 966993-934
NDC 1066993-934-54
NDC Item66993093454
DCSACIII
FDA SPL set id304583
LabelerPrasco Laboratories
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time high2019-02-12
Marketing effective time low2014-06-09
Marketing statusCOMPLETED
NDA_AUTHORIZED_GENERICNDA021454