"57237-222-01" National Drug Code (NDC)

NDC Code	57237-222-01
Package Description	100 CAPSULE in 1 BOTTLE (57237-222-01)
Product NDC	57237-222
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ramipril
Non-Proprietary Name	Ramipril
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20110608
Marketing Category Name	ANDA
Application Number	ANDA091604
Manufacturer	Rising Pharma Holdings, Inc.
Substance Name	RAMIPRIL
Strength	1.25
Strength Unit	mg/1
Pharmacy Classes	Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]