Norvasc - 0069-1530-41 - (AMLODIPINE BESYLATE)

Alphabetical Index


Drug Information of Norvasc

Product NDC: 0069-1530
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: 0069-1530
Labeler Name: Pfizer Laboratories Div Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019787
Marketing Category: NDA
Start Marketing Date: 19920731

Package Information of Norvasc

Package NDC: 0069-1530-41
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0069-1530-41) > 1 TABLET in 1 BLISTER PACK

NDC Information of Norvasc

NDC Code 0069-1530-41
Proprietary Name Norvasc
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0069-1530-41) > 1 TABLET in 1 BLISTER PACK
Product NDC 0069-1530
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 Pfizer Laboratories Div Pfizer 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