FDA.reportPublic FDA data

Application 208494

Type
ANDA
Sponsor
REYOUNG PHARMA CO LTD

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001SILDENAFIL CITRATESILDENAFIL CITRATETABLET;ORAL25MGNoNo
002SILDENAFIL CITRATESILDENAFIL CITRATETABLET;ORAL50MGNoNo
003SILDENAFIL CITRATESILDENAFIL CITRATETABLET;ORAL100MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
35561-251SildenafilsildenafilAustarPharma LLCANDACurrent
35561-252SildenafilsildenafilAustarPharma LLCANDACurrent
35561-253SildenafilsildenafilAustarPharma LLCANDACurrent
82647-210SildenafilsildenafilReyoung CorporationANDACurrent
82647-211SildenafilsildenafilReyoung CorporationANDACurrent
82647-212SildenafilsildenafilReyoung CorporationANDACurrent