"49349-729-02" National Drug Code (NDC)

NDC Code	49349-729-02
Package Description	30 TABLET in 1 BLISTER PACK (49349-729-02)
Product NDC	49349-729
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Fluconazole
Non-Proprietary Name	Fluconazole
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20110715
End Marketing Date	20171109
Marketing Category Name	ANDA
Application Number	ANDA076042
Manufacturer	REMEDYREPACK INC.
Substance Name	FLUCONAZOLE
Strength	150
Strength Unit	mg/1
Pharmacy Classes	Azole Antifungal [EPC],Azoles [Chemical/Ingredient],Cytochrome P450 2C19 Inhibitors [MoA],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 2C9 Inhibitors [MoA]