"16252-572-01" National Drug Code (NDC)

NDC Code	16252-572-01
Package Description	100 CAPSULE in 1 BOTTLE, PLASTIC (16252-572-01)
Product NDC	16252-572
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ramipril
Non-Proprietary Name	Ramipril
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20071226
End Marketing Date	20181231
Marketing Category Name	ANDA
Application Number	ANDA076549
Manufacturer	Actavis Pharma, Inc.
Substance Name	RAMIPRIL
Strength	5
Strength Unit	mg/1
Pharmacy Classes	Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]