Home > National Drug Code (NDC) > Amlodipine Besylate

Amlodipine Besylate - 68645-444-70 - (Amlodipine Besylate)

Alphabetical Index


Drug Information of Amlodipine Besylate

Product NDC: 68645-444
Proprietary Name: Amlodipine Besylate
Non Proprietary Name: Amlodipine Besylate
Active Ingredient(s): 5    mg/1 & nbsp;   Amlodipine Besylate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Amlodipine Besylate

Product NDC: 68645-444
Labeler Name: Legacy Pharmaceutical Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077995
Marketing Category: ANDA
Start Marketing Date: 20110101

Package Information of Amlodipine Besylate

Package NDC: 68645-444-70
Package Description: 30 TABLET in 1 BLISTER PACK (68645-444-70)

NDC Information of Amlodipine Besylate

NDC Code 68645-444-70
Proprietary Name Amlodipine Besylate
Package Description 30 TABLET in 1 BLISTER PACK (68645-444-70)
Product NDC 68645-444
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amlodipine Besylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110101
Marketing Category Name ANDA
Labeler Name Legacy Pharmaceutical Packaging
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 Besylate


General Information