abiraterone acetate
Generic: abiraterone acetate
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
abiraterone acetate
Generic Name
abiraterone acetate
Labeler
major pharmaceuticals
Dosage Form
TABLET
Routes
Active Ingredients
abiraterone acetate 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0904-6948
Product ID
0904-6948_d8b7c351-b030-4655-94af-f88ad6c5bd12
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208453
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
09046948
Hyphenated Format
0904-6948
Supplemental Identifiers
RxCUI
UNII
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 acetate (source: ndc)
Generic Name
abiraterone acetate (source: ndc)
Application Number
ANDA208453 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 30 BLISTER PACK in 1 CARTON (0904-6948-04) / 1 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d8b7c351-b030-4655-94af-f88ad6c5bd12", "openfda": {"unii": ["EM5OCB9YJ6"], "rxcui": ["1100075"], "spl_set_id": ["49809a29-6558-43a3-a347-5027de44aa41"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-6948-04) / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6948-04", "marketing_start_date": "20181123"}], "brand_name": "Abiraterone Acetate", "product_id": "0904-6948_d8b7c351-b030-4655-94af-f88ad6c5bd12", "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": "0904-6948", "generic_name": "Abiraterone Acetate", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Abiraterone Acetate", "active_ingredients": [{"name": "ABIRATERONE ACETATE", "strength": "250 mg/1"}], "application_number": "ANDA208453", "marketing_category": "ANDA", "marketing_start_date": "20181123", "listing_expiration_date": "20261231"}