Levitra - 54868-4967-3 - (vardenafil hydrochloride)

Alphabetical Index


Drug Information of Levitra

Product NDC: 54868-4967
Proprietary Name: Levitra
Non Proprietary Name: vardenafil hydrochloride
Active Ingredient(s): 20    mg/1 & nbsp;   vardenafil hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Levitra

Product NDC: 54868-4967
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021400
Marketing Category: NDA
Start Marketing Date: 20040127

Package Information of Levitra

Package NDC: 54868-4967-3
Package Description: 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4967-3)

NDC Information of Levitra

NDC Code 54868-4967-3
Proprietary Name Levitra
Package Description 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4967-3)
Product NDC 54868-4967
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name vardenafil hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040127
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name VARDENAFIL HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]

Complete Information of Levitra


General Information