Sildenafil - 60505-3404-9 - (Sildenafil)

Alphabetical Index


Drug Information of Sildenafil

Product NDC: 60505-3404
Proprietary Name: Sildenafil
Non Proprietary Name: Sildenafil
Active Ingredient(s): 20    mg/1 & nbsp;   Sildenafil
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Sildenafil

Product NDC: 60505-3404
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091379
Marketing Category: ANDA
Start Marketing Date: 20121106

Package Information of Sildenafil

Package NDC: 60505-3404-9
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (60505-3404-9)

NDC Information of Sildenafil

NDC Code 60505-3404-9
Proprietary Name Sildenafil
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (60505-3404-9)
Product NDC 60505-3404
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sildenafil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121106
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name SILDENAFIL CITRATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]

Complete Information of Sildenafil


General Information