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NDC properties for NDC 9 0299-6100

NDC item 00299610010

NDC 90299-6100
NDC 100299-6100-10
NDC Item00299610010
packaging1 TUBE in 1 CARTON (0299-6100-10) / 100 g in 1 TUBE
LabelerGalderma Laboratories, L.P.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2006-06-29
Marketing statusCOMPLETED
NDANDA021717

NDC item 00299610035

NDC 90299-6100
NDC 100299-6100-35
NDC Item00299610035
packaging1 TUBE in 1 CARTON (0299-6100-35) / 30 g in 1 TUBE
LabelerGalderma Laboratories, L.P.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2006-06-29
Marketing statusCOMPLETED
NDANDA021717

NDC item 51672530502

NDC 951672-5305
NDC 1051672-5305-2
NDC Item51672530502
packaging1 TUBE in 1 CARTON (51672-5305-2) / 30 g in 1 TUBE
LabelerSun Pharmaceutical Industries, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2018-12-11
Marketing statusCOMPLETED
NDANDA021717

NDC item 73575000902

NDC 973575-009
NDC 1073575-009-02
NDC Item73575000902
packaging2 TUBE in 1 CARTON (73575-009-02) / 30 g in 1 TUBE
LabelerOBA PHARMACEUTICALS INC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2020-01-24
Marketing statusCOMPLETED
NDANDA021717

NDC item 73575000904

NDC 973575-009
NDC 1073575-009-04
NDC Item73575000904
packaging4 TUBE in 1 CARTON (73575-009-04) / 30 g in 1 TUBE
LabelerOBA PHARMACEUTICALS INC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2020-01-24
Marketing statusCOMPLETED
NDANDA021717

NDC item 73575000909

NDC 973575-009
NDC 1073575-009-09
NDC Item73575000909
packaging1 TUBE in 1 CARTON (73575-009-09) / 30 g in 1 TUBE
LabelerOBA PHARMACEUTICALS INC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2020-01-24
Marketing statusCOMPLETED
NDANDA021717