PLENDIL - 63629-1596-1 - (Felodipine)

Alphabetical Index


Drug Information of PLENDIL

Product NDC: 63629-1596
Proprietary Name: PLENDIL
Non Proprietary Name: Felodipine
Active Ingredient(s): 10    mg/1 & nbsp;   Felodipine
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of PLENDIL

Product NDC: 63629-1596
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019834
Marketing Category: NDA
Start Marketing Date: 19910916

Package Information of PLENDIL

Package NDC: 63629-1596-1
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1596-1)

NDC Information of PLENDIL

NDC Code 63629-1596-1
Proprietary Name PLENDIL
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1596-1)
Product NDC 63629-1596
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Felodipine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19910916
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
Substance Name FELODIPINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of PLENDIL


General Information