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SILDENAFIL CITRATE - 13668-185-51 - (SILDENAFIL CITRATE)

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Drug Information of SILDENAFIL CITRATE

Product NDC: 13668-185
Proprietary Name: SILDENAFIL CITRATE
Non Proprietary Name: SILDENAFIL CITRATE
Active Ingredient(s): 20    mg/1 & nbsp;   SILDENAFIL CITRATE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of SILDENAFIL CITRATE

Product NDC: 13668-185
Labeler Name: Torrent Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091479
Marketing Category: ANDA
Start Marketing Date: 20121106

Package Information of SILDENAFIL CITRATE

Package NDC: 13668-185-51
Package Description: 5000 TABLET in 1 BOTTLE (13668-185-51)

NDC Information of SILDENAFIL CITRATE

NDC Code 13668-185-51
Proprietary Name SILDENAFIL CITRATE
Package Description 5000 TABLET in 1 BOTTLE (13668-185-51)
Product NDC 13668-185
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SILDENAFIL CITRATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121106
Marketing Category Name ANDA
Labeler Name Torrent Pharmaceuticals Limited
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 CITRATE


General Information