Product NDC: | 24236-287 |
Proprietary Name: | VIRACEPT |
Non Proprietary Name: | NELFINAVIR MESYLATE |
Active Ingredient(s): | 625 mg/1 & nbsp; NELFINAVIR MESYLATE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 24236-287 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021503 |
Marketing Category: | NDA |
Start Marketing Date: | 20130327 |
Package NDC: | 24236-287-21 |
Package Description: | 120 TABLET, FILM COATED in 1 CANISTER (24236-287-21) |
NDC Code | 24236-287-21 |
Proprietary Name | VIRACEPT |
Package Description | 120 TABLET, FILM COATED in 1 CANISTER (24236-287-21) |
Product NDC | 24236-287 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | NELFINAVIR MESYLATE |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20130327 |
Marketing Category Name | NDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | NELFINAVIR MESYLATE |
Strength Number | 625 |
Strength Unit | mg/1 |
Pharmaceutical Classes | HIV Protease Inhibitors [MoA],Protease Inhibitor [EPC] |