sildenafil - 55111-372-05 - (sildenafil)

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Drug Information of sildenafil

Product NDC: 55111-372
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: 55111-372
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202598
Marketing Category: ANDA
Start Marketing Date: 20121107

Package Information of sildenafil

Package NDC: 55111-372-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (55111-372-05)

NDC Information of sildenafil

NDC Code 55111-372-05
Proprietary Name sildenafil
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (55111-372-05)
Product NDC 55111-372
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sildenafil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121107
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories 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


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