"43063-802-90" National Drug Code (NDC)

NDC Code	43063-802-90
Package Description	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-802-90)
Product NDC	43063-802
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Spironolactone
Non-Proprietary Name	Spironolactone
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20060829
End Marketing Date	20210731
Marketing Category Name	ANDA
Application Number	ANDA040750
Manufacturer	PD-Rx Pharmaceuticals, Inc.
Substance Name	SPIRONOLACTONE
Strength	100
Strength Unit	mg/1
Pharmacy Classes	Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]