Amlodipine - 33342-015-12 - (Amlodipine)

Alphabetical Index


Drug Information of Amlodipine

Product NDC: 33342-015
Proprietary Name: Amlodipine
Non Proprietary Name: Amlodipine
Active Ingredient(s): 5    mg/1 & nbsp;   Amlodipine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Amlodipine

Product NDC: 33342-015
Labeler Name: Macleods Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201380
Marketing Category: ANDA
Start Marketing Date: 20120413

Package Information of Amlodipine

Package NDC: 33342-015-12
Package Description: 100 TABLET in 1 CARTON (33342-015-12)

NDC Information of Amlodipine

NDC Code 33342-015-12
Proprietary Name Amlodipine
Package Description 100 TABLET in 1 CARTON (33342-015-12)
Product NDC 33342-015
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amlodipine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120413
Marketing Category Name ANDA
Labeler Name Macleods Pharmaceuticals Limited
Substance Name AMLODIPINE BESYLATE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of Amlodipine


General Information