Ferrum Muriaticum Granules 1ch-30ch 1 Ch Tablet is a Health Canada–registered human drug (DIN 00769290) held by Dolisos Laboratoires S.a., containing Ferric Chloride. Health Canada lists its status as Cancelled Post Market (status date 09 Feb 1998). Nexara Health has matched 24 registrations of Ferric Chloride across 2 other regulated markets, 5 of them in the same strength and dosage form.
Health Canada registration
| DIN | 00769290 |
|---|---|
| Brand name | Ferrum Muriaticum Granules 1ch-30ch |
| Active ingredient | Ferric Chloride |
| Strength | 1 Ch |
| Dosage form | Tablet |
| Route | Oral |
| Company | Dolisos Laboratoires S.a. |
| Status | Cancelled Post Market — 09 Feb 1998 |
| Class | Human |
| ATC | |
| AHFS | 92:02.00* ; See footnote |
| Regulator record | Health Canada DPD entry · Product monograph |
Ferric Chloride registered in other markets
24 registrations of the same molecule in 2 national registries outside Canada (first 16 shown, exact strength and form first). Each row is taken from the regulator's own published list; status is shown as the registry reports it.
| Country | Product | Marketing authorisation holder | Strength | Form | Status | Registry |
|---|---|---|---|---|---|---|
| Taiwan | Ferromia | Sansho Co., Ltd. | 膜衣錠 | 已註銷 | TFDA | |
| Taiwan | FEXENOL Film Coated Tablet | 寶齡富錦生技股份有限公司平鎮廠 | 膜衣錠 | Registered | TFDA | |
| United States | Auryxia | Akebia Therapeutics, Inc. | Tablet, Film Coated | listed | FDA NDC | |
| United States | Ferric Citrate | Mylan Pharmaceuticals Inc. | Tablet, Film Coated | listed | FDA NDC | |
| United States | Ferric Citrate | Teva Pharmaceuticals, Inc. | Tablet, Film Coated | listed | FDA NDC | |
| Taiwan | Atofen Inj. | Uji Pharm. Co., Ltd. | 注射劑 | 已註銷 | TFDA | |
| Taiwan | Ferric Chloride Solution "Aid" | 健康化學製藥股份有限公司 | 外用液劑 | Registered | TFDA | |
| Taiwan | Ferric Chloride Solution "H.s.c." | 健康化學製藥股份有限公司 | 外用液劑 | 已註銷 | TFDA | |
| Taiwan | Gluferricon Injection | Nippon Zoki Pharmaceutical Co. Ltd. | 注射劑 | 已註銷 | TFDA | |
| Taiwan | Gluferricon Injection | Nippon Zoki Pharmaceutical Co. Ltd. | 注射劑 | 已註銷 | TFDA | |
| Taiwan | Helofer Ampoules | Hesses & Loss Helos O.h.g. | 注射劑 | 已註銷 | TFDA | |
| United States | Ferric citrate | Cohance Lifesciences Limited | Powder | FDA NDC | ||
| United States | Ferric citrate | Sionc Pharmaceuticals Pvt Ltd | Powder | FDA NDC | ||
| United States | Ferric Citrate | Nuray Chemicals Private Limited | Powder | FDA NDC | ||
| United States | Ferric Citrate | Siegfried USA, LLC | Powder | FDA NDC | ||
| United States | Ferric Citrate | Siegfried St. Vulbas SAS | Powder | FDA NDC |
See every manufacturer of Ferric Chloride worldwide →
Sourcing through Nexara Health
Nexara Health is a Health Canada–licensed wholesaler (DEL #3-002896) in Winnipeg. This DIN is not currently marketed in Canada. The registrations above show which regulated markets hold an equivalent presentation that can be sourced for clinical comparator use or on a named-patient basis under Health Canada's Special Access Programme. Request a quote or read how named-patient and foreign-pack supply works in Canada.
Frequently asked questions
Is Ferrum Muriaticum Granules 1ch-30ch (DIN 00769290) marketed in Canada?
No. Health Canada lists DIN 00769290 as Cancelled Post Market as of 09 Feb 1998.
Who holds the Canadian licence for this product?
Dolisos Laboratoires S.a. is the company of record in the Health Canada Drug Product Database.
Is Ferric Chloride registered outside Canada?
Yes — Nexara Health has matched 24 registrations in 2 other markets, including 5 in the same strength and dosage form (see the table above).
Where does this data come from?
Health Canada Drug Product Database (DPD), DIN 00769290, status date 1998-02-09; national medicine registries: FDA NDC, TFDA. Nexara Health re-checks these sources weekly and shows the last verification date at the top of the page.
Source: Health Canada Drug Product Database (DPD), DIN 00769290, status date 1998-02-09; national medicine registries: FDA NDC, TFDA.
Health Canada Drug Product Database (DPD), DIN 00769290, status date 1998-02-09; national medicine registries: FDA NDC, TFDA. Last reviewed 2026-09-17. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.