Cialis - 0002-4462-34 - (Tadalafil)

Alphabetical Index


Drug Information of Cialis

Product NDC: 0002-4462
Proprietary Name: Cialis
Non Proprietary Name: Tadalafil
Active Ingredient(s): 5    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: 0002-4462
Labeler Name: Eli Lilly and Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021368
Marketing Category: NDA
Start Marketing Date: 20031126

Package Information of Cialis

Package NDC: 0002-4462-34
Package Description: 2 BLISTER PACK in 1 CARTON (0002-4462-34) > 15 TABLET, FILM COATED in 1 BLISTER PACK (0002-4462-79)

NDC Information of Cialis

NDC Code 0002-4462-34
Proprietary Name Cialis
Package Description 2 BLISTER PACK in 1 CARTON (0002-4462-34) > 15 TABLET, FILM COATED in 1 BLISTER PACK (0002-4462-79)
Product NDC 0002-4462
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 Eli Lilly and Company
Substance Name TADALAFIL
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]

Complete Information of Cialis


General Information