abiraterone
Generic: abiraterone acetate
Labeler: civicascript, llcDrug Facts
Product Profile
Brand Name
abiraterone
Generic Name
abiraterone acetate
Labeler
civicascript, llc
Dosage Form
TABLET
Routes
Active Ingredients
abiraterone acetate 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
82249-010
Product ID
82249-010_e3758cee-2504-46be-8eb0-67463e7fe6ed
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208339
Listing Expiration
2026-12-31
Marketing Start
2018-11-23
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82249010
Hyphenated Format
82249-010
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
abiraterone (source: ndc)
Generic Name
abiraterone acetate (source: ndc)
Application Number
ANDA208339 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 120 TABLET in 1 BOTTLE, PLASTIC (82249-010-12)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e3758cee-2504-46be-8eb0-67463e7fe6ed", "openfda": {"upc": ["0382249010126"], "unii": ["EM5OCB9YJ6"], "rxcui": ["1100075"], "spl_set_id": ["0ef857ee-2bfc-4d27-a417-ad58fc3a6ff6"], "manufacturer_name": ["CivicaScript, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE, PLASTIC (82249-010-12)", "package_ndc": "82249-010-12", "marketing_start_date": "20220627"}], "brand_name": "Abiraterone", "product_id": "82249-010_e3758cee-2504-46be-8eb0-67463e7fe6ed", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 17A1 Inhibitor [EPC]", "Cytochrome P450 17A1 Inhibitors [MoA]", "Cytochrome P450 2C8 Inhibitors [MoA]", "Cytochrome P450 2D6 Inhibitors [MoA]"], "product_ndc": "82249-010", "generic_name": "Abiraterone acetate", "labeler_name": "CivicaScript, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Abiraterone", "active_ingredients": [{"name": "ABIRATERONE ACETATE", "strength": "250 mg/1"}], "application_number": "ANDA208339", "marketing_category": "ANDA", "marketing_start_date": "20181123", "listing_expiration_date": "20261231"}