CIALIS - 16590-905-10 - (TADALAFIL)

Alphabetical Index


Drug Information of CIALIS

Product NDC: 16590-905
Proprietary Name: CIALIS
Non Proprietary Name: TADALAFIL
Active Ingredient(s): 10    mg/1 & nbsp;   TADALAFIL
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of CIALIS

Product NDC: 16590-905
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021368
Marketing Category: NDA
Start Marketing Date: 20031126

Package Information of CIALIS

Package NDC: 16590-905-10
Package Description: 10 TABLET, FILM COATED in 1 BOTTLE (16590-905-10)

NDC Information of CIALIS

NDC Code 16590-905-10
Proprietary Name CIALIS
Package Description 10 TABLET, FILM COATED in 1 BOTTLE (16590-905-10)
Product NDC 16590-905
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TADALAFIL
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20031126
Marketing Category Name NDA
Labeler Name STAT RX USA LLC
Substance Name TADALAFIL
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]

Complete Information of CIALIS


General Information