Product NDC: | 52959-289 |
Proprietary Name: | VIRACEPT |
Non Proprietary Name: | nelfinavir mesylate |
Active Ingredient(s): | 250 mg/1 & nbsp; nelfinavir mesylate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52959-289 |
Labeler Name: | H.J. Harkins Company, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020779 |
Marketing Category: | NDA |
Start Marketing Date: | 19970314 |
Package NDC: | 52959-289-30 |
Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (52959-289-30) |
NDC Code | 52959-289-30 |
Proprietary Name | VIRACEPT |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (52959-289-30) |
Product NDC | 52959-289 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | nelfinavir mesylate |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 19970314 |
Marketing Category Name | NDA |
Labeler Name | H.J. Harkins Company, Inc. |
Substance Name | NELFINAVIR MESYLATE |
Strength Number | 250 |
Strength Unit | mg/1 |
Pharmaceutical Classes | HIV Protease Inhibitors [MoA],Protease Inhibitor [EPC] |