Product NDC: | 54868-0117 |
Proprietary Name: | ISENTRESS |
Non Proprietary Name: | RALTEGRAVIR |
Active Ingredient(s): | 400 mg/1 & nbsp; RALTEGRAVIR |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-0117 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022145 |
Marketing Category: | NDA |
Start Marketing Date: | 20080423 |
Package NDC: | 54868-0117-0 |
Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE (54868-0117-0) |
NDC Code | 54868-0117-0 |
Proprietary Name | ISENTRESS |
Package Description | 60 TABLET, FILM COATED in 1 BOTTLE (54868-0117-0) |
Product NDC | 54868-0117 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | RALTEGRAVIR |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20080423 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | RALTEGRAVIR POTASSIUM |
Strength Number | 400 |
Strength Unit | mg/1 |
Pharmaceutical Classes | HIV Integrase Inhibitors [MoA],Human Immunodeficiency Virus Integrase Strand Transfer Inhibitor [EPC] |