Ramipril - 31722-271-10 - (Ramipril)

Alphabetical Index


Drug Information of Ramipril

Product NDC: 31722-271
Proprietary Name: Ramipril
Non Proprietary Name: Ramipril
Active Ingredient(s): 1.25    mg/1 & nbsp;   Ramipril
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Ramipril

Product NDC: 31722-271
Labeler Name: Camber Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078745
Marketing Category: ANDA
Start Marketing Date: 20110101

Package Information of Ramipril

Package NDC: 31722-271-10
Package Description: 24 BOTTLE in 1 CASE (31722-271-10) > 1000 CAPSULE in 1 BOTTLE

NDC Information of Ramipril

NDC Code 31722-271-10
Proprietary Name Ramipril
Package Description 24 BOTTLE in 1 CASE (31722-271-10) > 1000 CAPSULE in 1 BOTTLE
Product NDC 31722-271
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ramipril
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110101
Marketing Category Name ANDA
Labeler Name Camber Pharmaceuticals
Substance Name RAMIPRIL
Strength Number 1.25
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Ramipril


General Information