"57237-090-01" National Drug Code (NDC)

NDC Code	57237-090-01
Package Description	100 TABLET in 1 BOTTLE (57237-090-01)
Product NDC	57237-090
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Trandolapril
Non-Proprietary Name	Trandolapril
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20070612
Marketing Category Name	ANDA
Application Number	ANDA078438
Manufacturer	Rising Pharma Holdings, Inc.
Substance Name	TRANDOLAPRIL
Strength	2
Strength Unit	mg/1
Pharmacy Classes	Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]