Product NDC: | 0006-0473 |
Proprietary Name: | ISENTRESS |
Non Proprietary Name: | RALTEGRAVIR |
Active Ingredient(s): | 25 mg/1 & nbsp; RALTEGRAVIR |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, CHEWABLE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0006-0473 |
Labeler Name: | Merck Sharp & Dohme Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA203045 |
Marketing Category: | NDA |
Start Marketing Date: | 20111221 |
Package NDC: | 0006-0473-61 |
Package Description: | 60 TABLET, CHEWABLE in 1 BOTTLE (0006-0473-61) |
NDC Code | 0006-0473-61 |
Proprietary Name | ISENTRESS |
Package Description | 60 TABLET, CHEWABLE in 1 BOTTLE (0006-0473-61) |
Product NDC | 0006-0473 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | RALTEGRAVIR |
Dosage Form Name | TABLET, CHEWABLE |
Route Name | ORAL |
Start Marketing Date | 20111221 |
Marketing Category Name | NDA |
Labeler Name | Merck Sharp & Dohme Corp. |
Substance Name | RALTEGRAVIR POTASSIUM |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes | HIV Integrase Inhibitors [MoA],Human Immunodeficiency Virus Integrase Strand Transfer Inhibitor [EPC] |