edurant
Generic: rilpivirine hydrochloride
Labeler: janssen products, lpDrug Facts
Product Profile
Brand Name
edurant
Generic Name
rilpivirine hydrochloride
Labeler
janssen products, lp
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
rilpivirine hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
59676-278
Product ID
59676-278_3d6d0fcc-0b62-b76b-e063-6294a90aea43
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA202022
Listing Expiration
2026-12-31
Marketing Start
2011-05-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59676278
Hyphenated Format
59676-278
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
edurant (source: ndc)
Generic Name
rilpivirine hydrochloride (source: ndc)
Application Number
NDA202022 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (59676-278-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3d6d0fcc-0b62-b76b-e063-6294a90aea43", "openfda": {"upc": ["0359676278016"], "unii": ["212WAX8KDD"], "rxcui": ["1102273", "1102277", "2678244", "2678248"], "spl_set_id": ["03880372-2c68-45c6-a53a-f420c49541d6"], "manufacturer_name": ["Janssen Products, LP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (59676-278-01)", "package_ndc": "59676-278-01", "marketing_start_date": "20110520"}], "brand_name": "EDURANT", "product_id": "59676-278_3d6d0fcc-0b62-b76b-e063-6294a90aea43", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]", "Non-Nucleoside Analog [EXT]", "Non-Nucleoside Reverse Transcriptase Inhibitors [MoA]"], "product_ndc": "59676-278", "generic_name": "rilpivirine hydrochloride", "labeler_name": "Janssen Products, LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "EDURANT", "active_ingredients": [{"name": "RILPIVIRINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "NDA202022", "marketing_category": "NDA", "marketing_start_date": "20110520", "listing_expiration_date": "20261231"}