Package 16714-963-01

Brand: abiraterone acetate

Generic: abiraterone acetate
NDC Package

Package Facts

Identity

Package NDC 16714-963-01
Digits Only 1671496301
Product NDC 16714-963
Description

120 TABLET in 1 BOTTLE (16714-963-01)

Marketing

Marketing Status
Marketed Since 2020-05-19
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": "564a91be-2efd-3ec5-1996-1491749f271e", "openfda": {"unii": ["EM5OCB9YJ6"], "rxcui": ["1100075"], "spl_set_id": ["39434b24-bf64-f5c9-fbb6-b0d225099424"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (16714-963-01)", "package_ndc": "16714-963-01", "marketing_start_date": "20200519"}], "brand_name": "Abiraterone Acetate", "product_id": "16714-963_564a91be-2efd-3ec5-1996-1491749f271e", "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": "16714-963", "generic_name": "Abiraterone Acetate", "labeler_name": "NorthStar Rx LLC", "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": "20200519", "listing_expiration_date": "20261231"}