Amlobenz - 63629-1454-1 - (Amlobenz)

Alphabetical Index


Drug Information of Amlobenz

Product NDC: 63629-1454
Proprietary Name: Amlobenz
Non Proprietary Name: Amlobenz
Active Ingredient(s): 5; 20    mg/1; mg/1 & nbsp;   Amlobenz
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Amlobenz

Product NDC: 63629-1454
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077183
Marketing Category: ANDA
Start Marketing Date: 20100419

Package Information of Amlobenz

Package NDC: 63629-1454-1
Package Description: 30 CAPSULE in 1 BOTTLE (63629-1454-1)

NDC Information of Amlobenz

NDC Code 63629-1454-1
Proprietary Name Amlobenz
Package Description 30 CAPSULE in 1 BOTTLE (63629-1454-1)
Product NDC 63629-1454
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amlobenz
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100419
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Strength Number 5; 20
Strength Unit mg/1; mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]

Complete Information of Amlobenz


General Information