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ISENTRESS
ISENTRESS - 0006-0227-61 - (RALTEGRAVIR)
Drug Information of ISENTRESS
| Product NDC: | 0006-0227 |
| 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) |
Labeler Information of ISENTRESS
| Product NDC: | 0006-0227 |
| Labeler Name: | Merck Sharp & Dohme Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022145 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20071012 |
Package Information of ISENTRESS
| Package NDC: | 0006-0227-61 |
| Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE (0006-0227-61) |
NDC Information of ISENTRESS
| NDC Code | 0006-0227-61 |
| Proprietary Name | ISENTRESS |
| Package Description | 60 TABLET, FILM COATED in 1 BOTTLE (0006-0227-61) |
| Product NDC | 0006-0227 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | RALTEGRAVIR |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20071012 |
| Marketing Category Name | NDA |
| Labeler Name | Merck Sharp & Dohme Corp. |
| 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] |
