Revatio - 55154-2729-0 - (sildenafil citrate)

Alphabetical Index


Drug Information of Revatio

Product NDC: 55154-2729
Proprietary Name: Revatio
Non Proprietary Name: sildenafil citrate
Active Ingredient(s): 20    mg/1 & nbsp;   sildenafil citrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Revatio

Product NDC: 55154-2729
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021845
Marketing Category: NDA
Start Marketing Date: 20050603

Package Information of Revatio

Package NDC: 55154-2729-0
Package Description: 10 POUCH in 1 BAG (55154-2729-0) > 1 TABLET, FILM COATED in 1 POUCH

NDC Information of Revatio

NDC Code 55154-2729-0
Proprietary Name Revatio
Package Description 10 POUCH in 1 BAG (55154-2729-0) > 1 TABLET, FILM COATED in 1 POUCH
Product NDC 55154-2729
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sildenafil citrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20050603
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name SILDENAFIL CITRATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]

Complete Information of Revatio


General Information