Product NDC: | 0002-4465 |
Proprietary Name: | Cialis |
Non Proprietary Name: | Tadalafil |
Active Ingredient(s): | 2.5 mg/1 & nbsp; Tadalafil |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0002-4465 |
Labeler Name: | Eli Lilly and Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021368 |
Marketing Category: | NDA |
Start Marketing Date: | 20080107 |
Package NDC: | 0002-4465-34 |
Package Description: | 2 BLISTER PACK in 1 CARTON (0002-4465-34) > 15 TABLET, FILM COATED in 1 BLISTER PACK (0002-4465-79) |
NDC Code | 0002-4465-34 |
Proprietary Name | Cialis |
Package Description | 2 BLISTER PACK in 1 CARTON (0002-4465-34) > 15 TABLET, FILM COATED in 1 BLISTER PACK (0002-4465-79) |
Product NDC | 0002-4465 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Tadalafil |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20080107 |
Marketing Category Name | NDA |
Labeler Name | Eli Lilly and Company |
Substance Name | TADALAFIL |
Strength Number | 2.5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA] |