Ramipril - 21695-821-30 - (ramipril)

Alphabetical Index


Drug Information of Ramipril

Product NDC: 21695-821
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: 21695-821
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076549
Marketing Category: ANDA
Start Marketing Date: 20071226

Package Information of Ramipril

Package NDC: 21695-821-30
Package Description: 30 CAPSULE in 1 BOTTLE (21695-821-30)

NDC Information of Ramipril

NDC Code 21695-821-30
Proprietary Name Ramipril
Package Description 30 CAPSULE in 1 BOTTLE (21695-821-30)
Product NDC 21695-821
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ramipril
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20071226
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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