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NDC properties for NDC 9 0065-0644

NDC item 00065064435

NDC 90065-0644
NDC 100065-0644-35
NDC Item00065064435
packaging3.5 g in 1 TUBE (0065-0644-35)
FDA SPL set id691162
LabelerAlcon Laboratories, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time high2023-07-31
Marketing effective time low1981-06-28
Marketing statusCOMPLETED
NDANDA050555

NDC item 00078081301

NDC 90078-0813
NDC 100078-0813-01
NDC Item00078081301
packaging3.5 g in 1 TUBE (0078-0813-01)
FDA SPL set id861855
LabelerNovartis Pharmaceuticals Corporation
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low1981-06-28
Marketing statusACTIVE
NDANDA050555

NDC item 00247088181

NDC 10UNKNOWN
NDC Item00247088181

NDC item 49999025935

NDC 949999-259
NDC 1049999-259-35
NDC Item49999025935

NDC item 52959005101

NDC 10UNKNOWN
NDC Item52959005101

NDC item 52959005103

NDC 10UNKNOWN
NDC Item52959005103

NDC item 68071133505

NDC 968071-1335
NDC 1068071-1335-5
NDC Item68071133505