Product NDC: | 0002-5123 |
Proprietary Name: | Effient |
Non Proprietary Name: | Prasugrel hydrochloride |
Active Ingredient(s): | 10 mg/1 & nbsp; Prasugrel hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0002-5123 |
Labeler Name: | Eli Lilly and Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022307 |
Marketing Category: | NDA |
Start Marketing Date: | 20120301 |
Package NDC: | 0002-5123-77 |
Package Description: | 90 BLISTER PACK in 1 CARTON (0002-5123-77) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0002-5123-01) |
NDC Code | 0002-5123-77 |
Proprietary Name | Effient |
Package Description | 90 BLISTER PACK in 1 CARTON (0002-5123-77) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0002-5123-01) |
Product NDC | 0002-5123 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Prasugrel hydrochloride |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20120301 |
Marketing Category Name | NDA |
Labeler Name | Eli Lilly and Company |
Substance Name | PRASUGREL HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Decreased Platelet Aggregation [PE],P2Y12 Platelet Inhibitor [EPC],P2Y12 Receptor Antagonists [MoA] |