Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Akebia Therapeutics, Inc. names for other drugs.
Recalls
- Mar 15, 2021 · Class II · Cardinal Health Inc.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots: AN0142D - Dec 9, 2020 · Class II · Akebia Therapeutics dba Keryx Biopharmaceutials, Inc
CGMP Deviations
Lots: Lot Number: 9062, exp. date Feb 2021 - Jul 10, 2020 · Class II · Keryx Biopharmaceuticals, Inc.
cGMP deviations: Lots recalled were not manufactured in conformance with the FDA-approved manufacturing process for Auryxia.
Lots: Lot #s: AK6003C, Exp. 10/31/2020; AK6004B, Exp. 11/30/2020; CBMKF, CBMKH, Exp. 08/31/2020; CCKSM, Exp. 09/30/2020; CBWKN, Exp. 11/30/2020; CCSTZ, CCWZB, Exp. 05/31/2021; CCYSF, CCYSG, CCWZC, Exp. 06/30/2021; CDCTB, CDCSZ, Exp. 07/31/2021. - Dec 12, 2017 · Class III · Keryx Biopharmaceuticals, Inc.
Presence of Foreign Substance: Reports have been received of damaged StripPax packets containing silica gel desiccant potentially allowing the silica gel granules to make contact with Auryxia tablets in the bottle.
Lots: Lot # AH3842
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ferric Cation: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 210 mg
- Approval
- NDA NDA205874
- On the market since
- Sep 17, 2014
- Package NDCs
59922-631-01- Official label
- DailyMed (National Library of Medicine), updated Oct 29, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?