Package 71921-178-20

Brand: abiraterone acetate

Generic: abiraterone acetate
NDC Package

Package Facts

Identity

Package NDC 71921-178-20
Digits Only 7192117820
Product NDC 71921-178
Description

120 TABLET in 1 BOTTLE (71921-178-20)

Marketing

Marketing Status
Marketed Since 2022-08-15
Brand abiraterone acetate
Generic abiraterone acetate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38b4b689-c306-42a0-9df6-5b125314aaab", "openfda": {"upc": ["0371921178209"], "unii": ["EM5OCB9YJ6"], "rxcui": ["1100075"], "spl_set_id": ["b3e7f851-4132-4003-8f14-0eea21e5009c"], "manufacturer_name": ["Florida Pharmaceutical Products, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (71921-178-20)", "package_ndc": "71921-178-20", "marketing_start_date": "20220815"}], "brand_name": "abiraterone acetate", "product_id": "71921-178_38b4b689-c306-42a0-9df6-5b125314aaab", "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": "71921-178", "generic_name": "abiraterone acetate", "labeler_name": "Florida Pharmaceutical Products, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "abiraterone acetate", "active_ingredients": [{"name": "ABIRATERONE ACETATE", "strength": "250 mg/1"}], "application_number": "ANDA212462", "marketing_category": "ANDA", "marketing_start_date": "20220815", "listing_expiration_date": "20261231"}