Ramipril - 35356-893-60 - (Ramipril)

Alphabetical Index


Drug Information of Ramipril

Product NDC: 35356-893
Proprietary Name: Ramipril
Non Proprietary Name: Ramipril
Active Ingredient(s): 10    mg/1 & nbsp;   Ramipril
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Ramipril

Product NDC: 35356-893
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077470
Marketing Category: ANDA
Start Marketing Date: 20080624

Package Information of Ramipril

Package NDC: 35356-893-60
Package Description: 60 CAPSULE in 1 BOTTLE (35356-893-60)

NDC Information of Ramipril

NDC Code 35356-893-60
Proprietary Name Ramipril
Package Description 60 CAPSULE in 1 BOTTLE (35356-893-60)
Product NDC 35356-893
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ramipril
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20080624
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name RAMIPRIL
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Ramipril


General Information