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NDC properties for NDC 9 69420-3077

NDC item 69420307701

NDC 969420-3077
NDC 1069420-3077-1
NDC Item69420307701
packaging30 g in 1 TUBE, WITH APPLICATOR (69420-3077-1)
FDA SPL set id510238
LabelerSA3, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time high2022-07-31
Marketing effective time low2020-03-13
Marketing statusCOMPLETED
NDA_AUTHORIZED_GENERICNDA021717

NDC item 71800063104

NDC 971800-631
NDC 1071800-631-04
NDC Item71800063104
packaging4 TUBE in 1 CARTON (71800-631-04) / 30 g in 1 TUBE
FDA SPL set id591823
LabelerInnovida Pharmaceutique Corporation
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2017-05-03
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA021717

NDC item 71800063108

NDC 971800-631
NDC 1071800-631-08
NDC Item71800063108
packaging8 TUBE in 1 CARTON (71800-631-08) / 30 g in 1 TUBE
FDA SPL set id591823
LabelerInnovida Pharmaceutique Corporation
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2017-05-03
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA021717

NDC item 71800063115

NDC 971800-631
NDC 1071800-631-15
NDC Item71800063115
packaging1 TUBE in 1 CARTON (71800-631-15) / 30 g in 1 TUBE
FDA SPL set id591823
LabelerInnovida Pharmaceutique Corporation
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2017-05-03
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA021717