"68084-552-21" National Drug Code (NDC)

NDC Code	68084-552-21
Package Description	30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-552-21) > 1 TABLET in 1 BLISTER PACK (68084-552-11)
Product NDC	68084-552
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ketoconazole
Non-Proprietary Name	Ketoconazole
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20111221
End Marketing Date	20190531
Marketing Category Name	ANDA
Application Number	ANDA075597
Manufacturer	American Health Packaging
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]