Ramipril - 0093-7437-01 - (Ramipril)

Alphabetical Index


Drug Information of Ramipril

Product NDC: 0093-7437
Proprietary Name: Ramipril
Non Proprietary Name: Ramipril
Active Ingredient(s): 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: 0093-7437
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077470
Marketing Category: ANDA
Start Marketing Date: 20080624

Package Information of Ramipril

Package NDC: 0093-7437-01
Package Description: 100 CAPSULE in 1 BOTTLE (0093-7437-01)

NDC Information of Ramipril

NDC Code 0093-7437-01
Proprietary Name Ramipril
Package Description 100 CAPSULE in 1 BOTTLE (0093-7437-01)
Product NDC 0093-7437
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 Teva Pharmaceuticals USA Inc
Substance Name RAMIPRIL
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Ramipril


General Information