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"53808-0842-1" National Drug Code (NDC)
Ketoconazole 30 TABLET in 1 BLISTER PACK (53808-0842-1)
(State of Florida DOH Central Pharmacy)
NDC Code
53808-0842-1
Package Description
30 TABLET in 1 BLISTER PACK (53808-0842-1)
Product NDC
53808-0842
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ketoconazole
Non-Proprietary Name
Ketoconazole
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20130101
Marketing Category Name
ANDA
Application Number
ANDA075597
Manufacturer
State of Florida DOH Central Pharmacy
Substance Name
KETOCONAZOLE
Strength
200
Strength Unit
mg/1
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/53808-0842-1