Package 59922-631-01

Brand: auryxia

Generic: ferric citrate
NDC Package

Package Facts

Identity

Package NDC 59922-631-01
Digits Only 5992263101
Product NDC 59922-631
Product ID 59922-631_79cb63af-94fa-4f49-91d3-543c0058cd4e
Description

200 TABLET, FILM COATED in 1 BOTTLE (59922-631-01)

Marketing

Marketing Status
Marketed Since 2014-09-17
Brand auryxia
Generic ferric citrate
Sample Package No

Linked Drug Pages (1)

Auryxia ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "79cb63af-94fa-4f49-91d3-543c0058cd4e", "openfda": {"unii": ["Q91187K011"], "rxcui": ["1594680", "1596023"], "spl_set_id": ["aadd18e0-3752-11e4-8510-0800200c9a66"], "manufacturer_name": ["Akebia Therapeutics, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET, FILM COATED in 1 BOTTLE (59922-631-01)", "package_ndc": "59922-631-01", "marketing_start_date": "20140917"}], "brand_name": "Auryxia", "product_id": "59922-631_79cb63af-94fa-4f49-91d3-543c0058cd4e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Iron [CS]", "Parenteral Iron Replacement [EPC]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "59922-631", "generic_name": "ferric citrate", "labeler_name": "Akebia Therapeutics, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Auryxia", "active_ingredients": [{"name": "TETRAFERRIC TRICITRATE DECAHYDRATE", "strength": "210 mg/1"}], "application_number": "NDA205874", "marketing_category": "NDA", "marketing_start_date": "20140917", "listing_expiration_date": "20261231"}