"87722-069-01" National Drug Code (NDC)

Anti Dandruff 200 mg in 1 BOTTLE (87722-069-01)
(Guangdong Jiaoyu Biotechnology Co., Ltd)

NDC Code87722-069-01
Package Description200 mg in 1 BOTTLE (87722-069-01)
Product NDC87722-069
Product Type NameHUMAN OTC DRUG
Proprietary NameAnti Dandruff
Non-Proprietary NameKetoconazole
Dosage FormLIQUID
UsageTOPICAL
Start Marketing Date20261003
Marketing Category NameOTC MONOGRAPH DRUG
Application NumberM032
ManufacturerGuangdong Jiaoyu Biotechnology Co., Ltd
Substance NameKETOCONAZOLE
Strength1
Strength Unitmg/100mg
Pharmacy ClassesAzole Antifungal [EPC], Azoles [CS], Cytochrome P450 3A4 Inhibitors [MoA], Cytochrome P450 3A5 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]

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