SELZENTRY - 49702-216-18 - (maraviroc)

Alphabetical Index


Drug Information of SELZENTRY

Product NDC: 49702-216
Proprietary Name: SELZENTRY
Non Proprietary Name: maraviroc
Active Ingredient(s): 300    mg/1 & nbsp;   maraviroc
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of SELZENTRY

Product NDC: 49702-216
Labeler Name: ViiV Healthcare Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022128
Marketing Category: NDA
Start Marketing Date: 20100901

Package Information of SELZENTRY

Package NDC: 49702-216-18
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (49702-216-18)

NDC Information of SELZENTRY

NDC Code 49702-216-18
Proprietary Name SELZENTRY
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (49702-216-18)
Product NDC 49702-216
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name maraviroc
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100901
Marketing Category Name NDA
Labeler Name ViiV Healthcare Company
Substance Name MARAVIROC
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes CCR5 Co-receptor Antagonist [EPC],Chemokine Co-receptor 5 Antagonists [MoA]

Complete Information of SELZENTRY


General Information