Generic Triferic Availability
Last updated on Jun 11, 2025.
Triferic is a brand name of ferric pyrophosphate, approved by the FDA in the following formulation(s):
TRIFERIC (ferric pyrophosphate citrate - powder;intravenous)
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Manufacturer: ROCKWELL MEDICAL INC
Approval date: April 25, 2016
Strength(s): 272MG IRON/PACKET (discontinued) [RLD]
TRIFERIC (ferric pyrophosphate citrate - solution;intravenous)
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Manufacturer: ROCKWELL MEDICAL INC
Approval date: January 23, 2015
Strength(s): 27.2MG IRON/5ML (5.44MG IRON/ML) (discontinued) [RLD] -
Manufacturer: ROCKWELL MEDICAL INC
Approval date: September 4, 2015
Strength(s): 272MG IRON/50ML (5.44MG IRON/ML) (discontinued) [RLD]
All of the above formulations have been discontinued.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Triferic. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.
See also: Generic Drug FAQ.
Related patents
Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.
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Methods for the preparation and use of ferric pyrophosphate citrate chelate compositions
Patent 7,816,404
Issued: October 19, 2010
Inventor(s): McCall, Jr.; William S.
Assignee(s): Rockwell Medical Technologies, Inc. (Wixom, MI)A highly water soluble ferric pyrophosphate citrate chelate useful for treating iron deficiency contains 2% or less phosphate by weight. These chelate compositions are easily milled and/or processed into dosage forms using conventional techniques, and are expected to exhibit advantageous biocompatibility as compared to conventional soluble ferric pyrophosphates, ferric salts, ferric polysaccharide complexes and ferrous salts.
Patent expiration dates:
- April 17, 2029✓
- April 17, 2029✓✓
- April 17, 2029
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Packaging of ferric pyrophosphate for dialysis
Patent 7,857,977
Issued: December 28, 2010
Inventor(s): Wash; Lori L.
Assignee(s): Rockwell Medical Technologies, Inc. (Wixom, MI)A stable packaged bicarbonate solution for use in dialysis treatment and for treating anemia, iron deficiency, or reducing the required dose of recombinant erythropoietin to treat anemia includes a bicarbonate solution into which ferric pyrophosphate is dissolved. The amount of ferric pyrophosphate dissolved in the bicarbonate solution is sufficient to provide a therapeutic effect for the treatment of anemia, iron deficiency or to reduce dose of recombinant erythropoietin needed to treat anemia when the bicarbonate solution is combined with other dialysis components to form a dialysate used for dialyzing a patient. The ferric pyrophosphate is stabilized in the bicarbonate solution by holding the solution in a polyolefin container or container liner, such as a high density polyethylene container or liner.
Patent expiration dates:
- September 8, 2027✓
- September 8, 2027
More about Triferic (ferric pyrophosphate)
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- Reviews (1)
- Side effects
- Dosage information
- During pregnancy
- FDA approval history
- Drug class: iron products
- Breastfeeding
- En español
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Glossary
Term | Definition |
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Drug Patent | A drug patent is assigned by the U.S. Patent and Trademark Office and assigns exclusive legal right to the patent holder to protect the proprietary chemical formulation. The patent assigns exclusive legal right to the inventor or patent holder, and may include entities such as the drug brand name, trademark, product dosage form, ingredient formulation, or manufacturing process A patent usually expires 20 years from the date of filing, but can be variable based on many factors, including development of new formulations of the original chemical, and patent infringement litigation. |
Drug Exclusivity | Exclusivity is the sole marketing rights granted by the FDA to a manufacturer upon the approval of a drug and may run simultaneously with a patent. Exclusivity periods can run from 180 days to seven years depending upon the circumstance of the exclusivity grant. |
RLD | A Reference Listed Drug (RLD) is an approved drug product to which new generic versions are compared to show that they are bioequivalent. A drug company seeking approval to market a generic equivalent must refer to the Reference Listed Drug in its Abbreviated New Drug Application (ANDA). By designating a single reference listed drug as the standard to which all generic versions must be shown to be bioequivalent, FDA hopes to avoid possible significant variations among generic drugs and their brand name counterpart. |
Further information
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