Package 0143-9597-21

Brand: abiraterone

Generic: abiraterone acetate
NDC Package

Package Facts

Identity

Package NDC 0143-9597-21
Digits Only 0143959721
Product NDC 0143-9597
Description

120 TABLET in 1 BOTTLE (0143-9597-21)

Marketing

Marketing Status
Marketed Since 2018-11-23
Brand abiraterone
Generic abiraterone acetate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "35e5846f-9299-4190-94bb-6b0bb0d92485", "openfda": {"upc": ["0301439597216"], "unii": ["EM5OCB9YJ6"], "rxcui": ["1100075"], "spl_set_id": ["be29365a-ed25-44c0-9818-e9016dc95ba6"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (0143-9597-21)", "package_ndc": "0143-9597-21", "marketing_start_date": "20181123"}], "brand_name": "Abiraterone", "product_id": "0143-9597_35e5846f-9299-4190-94bb-6b0bb0d92485", "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": "0143-9597", "generic_name": "Abiraterone acetate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "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"}