abiraterone acetate
Generic: abiraterone acetate
Labeler: dr. reddys laboratories incDrug Facts
Product Profile
Brand Name
abiraterone acetate
Generic Name
abiraterone acetate
Labeler
dr. reddys laboratories inc
Dosage Form
TABLET
Routes
Active Ingredients
abiraterone acetate 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
75907-224
Product ID
75907-224_6c96e35d-9099-e164-0960-353b01420f81
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208416
Listing Expiration
2026-12-31
Marketing Start
2025-03-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
75907224
Hyphenated Format
75907-224
Supplemental Identifiers
RxCUI
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 acetate (source: ndc)
Generic Name
abiraterone acetate (source: ndc)
Application Number
ANDA208416 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 120 TABLET in 1 BOTTLE (75907-224-04)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6c96e35d-9099-e164-0960-353b01420f81", "openfda": {"unii": ["EM5OCB9YJ6"], "rxcui": ["1100075"], "spl_set_id": ["0c91aa38-3b0a-232c-8eb1-55f08e8e6644"], "manufacturer_name": ["Dr. Reddys Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (75907-224-04)", "package_ndc": "75907-224-04", "marketing_start_date": "20250317"}], "brand_name": "Abiraterone Acetate", "product_id": "75907-224_6c96e35d-9099-e164-0960-353b01420f81", "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": "75907-224", "generic_name": "Abiraterone Acetate", "labeler_name": "Dr. Reddys Laboratories Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Abiraterone Acetate", "active_ingredients": [{"name": "ABIRATERONE ACETATE", "strength": "250 mg/1"}], "application_number": "ANDA208416", "marketing_category": "ANDA", "marketing_start_date": "20250317", "listing_expiration_date": "20261231"}