Product NDC: | 0002-4463 |
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) |
Product NDC: | 0002-4463 |
Labeler Name: | Eli Lilly and Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021368 |
Marketing Category: | NDA |
Start Marketing Date: | 20031126 |
Package NDC: | 0002-4463-63 |
Package Description: | 1 BLISTER PACK in 1 CARTON (0002-4463-63) > 3 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Code | 0002-4463-63 |
Proprietary Name | Cialis |
Package Description | 1 BLISTER PACK in 1 CARTON (0002-4463-63) > 3 TABLET, FILM COATED in 1 BLISTER PACK |
Product NDC | 0002-4463 |
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 | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA] |