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FELODIPINEEXTENDED-RELEASE TABLETS - 63304-435-01 - (felodipine)

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Drug Information of FELODIPINEEXTENDED-RELEASE TABLETS

Product NDC: 63304-435
Proprietary Name: FELODIPINEEXTENDED-RELEASE TABLETS
Non Proprietary Name: felodipine
Active Ingredient(s): 2.5    mg/1 & nbsp;   felodipine
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of FELODIPINEEXTENDED-RELEASE TABLETS

Product NDC: 63304-435
Labeler Name: Ranbaxy Pharmaceuticals Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019834
Marketing Category: NDA
Start Marketing Date: 20080910

Package Information of FELODIPINEEXTENDED-RELEASE TABLETS

Package NDC: 63304-435-01
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-435-01)

NDC Information of FELODIPINEEXTENDED-RELEASE TABLETS

NDC Code 63304-435-01
Proprietary Name FELODIPINEEXTENDED-RELEASE TABLETS
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-435-01)
Product NDC 63304-435
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name felodipine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20080910
Marketing Category Name NDA
Labeler Name Ranbaxy Pharmaceuticals Inc
Substance Name FELODIPINE
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of FELODIPINEEXTENDED-RELEASE TABLETS


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