"72789-096-02" National Drug Code (NDC)

NDC Code	72789-096-02
Package Description	2 TABLET in 1 BOTTLE, PLASTIC (72789-096-02)
Product NDC	72789-096
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Fluconazole
Non-Proprietary Name	Fluconazole
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20170224
End Marketing Date	20230731
Marketing Category Name	ANDA
Application Number	ANDA078423
Manufacturer	PD-Rx Pharmaceuticals, Inc.
Substance Name	FLUCONAZOLE
Strength	150
Strength Unit	mg/1
Pharmacy Classes	Azole Antifungal [EPC], Azoles [CS], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA]