Amlobenz - 21695-916-30 - (Amlobenz)

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Drug Information of Amlobenz

Product NDC: 21695-916
Proprietary Name: Amlobenz
Non Proprietary Name: Amlobenz
Active Ingredient(s): 10; 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: 21695-916
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077183
Marketing Category: ANDA
Start Marketing Date: 20100419

Package Information of Amlobenz

Package NDC: 21695-916-30
Package Description: 30 CAPSULE in 1 BOTTLE (21695-916-30)

NDC Information of Amlobenz

NDC Code 21695-916-30
Proprietary Name Amlobenz
Package Description 30 CAPSULE in 1 BOTTLE (21695-916-30)
Product NDC 21695-916
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 Rebel Distributors Corp
Substance Name AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Strength Number 10; 20
Strength Unit mg/1; mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE],Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of Amlobenz


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