Ramipril - 65862-475-99 - (Ramipril)

Alphabetical Index


Drug Information of Ramipril

Product NDC: 65862-475
Proprietary Name: Ramipril
Non Proprietary Name: Ramipril
Active Ingredient(s): 2.5    mg/1 & nbsp;   Ramipril
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Ramipril

Product NDC: 65862-475
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091604
Marketing Category: ANDA
Start Marketing Date: 20110608

Package Information of Ramipril

Package NDC: 65862-475-99
Package Description: 1000 CAPSULE in 1 BOTTLE (65862-475-99)

NDC Information of Ramipril

NDC Code 65862-475-99
Proprietary Name Ramipril
Package Description 1000 CAPSULE in 1 BOTTLE (65862-475-99)
Product NDC 65862-475
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ramipril
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110608
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name RAMIPRIL
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Ramipril


General Information