Norvasc - 55289-103-60 - (amlodipine besylate)

Alphabetical Index


Drug Information of Norvasc

Product NDC: 55289-103
Proprietary Name: Norvasc
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 Norvasc

Product NDC: 55289-103
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019787
Marketing Category: NDA
Start Marketing Date: 19920731

Package Information of Norvasc

Package NDC: 55289-103-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (55289-103-60)

NDC Information of Norvasc

NDC Code 55289-103-60
Proprietary Name Norvasc
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (55289-103-60)
Product NDC 55289-103
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amlodipine besylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19920731
Marketing Category Name NDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
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 Norvasc


General Information