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"87722-069-01" National Drug Code (NDC)
Anti Dandruff 200 mg in 1 BOTTLE (87722-069-01)
(Guangdong Jiaoyu Biotechnology Co., Ltd)
NDC Code
87722-069-01
Package Description
200 mg in 1 BOTTLE (87722-069-01)
Product NDC
87722-069
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Anti Dandruff
Non-Proprietary Name
Ketoconazole
Dosage Form
LIQUID
Usage
TOPICAL
Start Marketing Date
20261003
Marketing Category Name
OTC MONOGRAPH DRUG
Application Number
M032
Manufacturer
Guangdong Jiaoyu Biotechnology Co., Ltd
Substance Name
KETOCONAZOLE
Strength
1
Strength Unit
mg/100mg
Pharmacy Classes
Azole Antifungal [EPC], Azoles [CS], Cytochrome P450 3A4 Inhibitors [MoA], Cytochrome P450 3A5 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/87722-069-01