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Marc-Blast Lyophilized Powder

NAFDAC Reg. No. A6-100130 · Drug

Registered with NAFDAC — registration activeAs of 5 November 2026 · synced automatically from official sources.
Product
Marc-Blast Lyophilized Powder
NAFDAC number
A6-100130
Active ingredient
Trafermin
Strength
7000 IU/Vial
Form
Powder
Pack size
70000 IU x 1's (in vial)
Manufacturer
Not listed
Applicant (holder)
Marcson Healthcare Limited
Approved
5 Nov 2023
Status
Active View on NAFDAC ↗
Registration valid to
30 Oct 2028
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • Marc-Blast Lyophilized Powder is on the NAFDAC register with an active registration (A6-100130). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. Not medical advice — always follow your doctor or pharmacist.

What Marc-Blast Lyophilized Powder is used for

From the official U.S. FDA label for Marc-Blast Lyophilized Powder, the active ingredient registered with NAFDAC.

Boxed warning: PERI-PROCEDURAL COMPLICATIONS, MYELOSUPPRESSION Severe peri-procedural complications including hemorrhage, hepatocellular injury, and thromboembolic events may occur via hepatic intra-arterial administration of HEPZATO. Assess patients for these adverse reactions during and for at least 72 hours following administration of HEPZATO [see Warnings and Precautions ( 5.1 )]. …
What it is used for

HEPZATO for injection, as a component of the HEPZATO KIT, is indicated as a liver-directed treatment for adult patients with uveal melanoma with unresectable hepatic metastases affecting less than 50% of the liver and no extrahepatic disease or extrahepatic disease limited to the bone, lymph nodes, subcutaneous tissues, or lung that is amenable to resection or radiation. …

Possible side effects

Below are adverse reactions associated with HEPZATO KIT. Additional adverse reactions related to the procedure and/or medical device are described in further detail in the HEPZATO KIT IFU. The following clinically significant adverse reactions are described elsewhere in the labeling: Peri-procedural complications [see Warnings and Precautions ( 5.1 )] Myelosuppression [see Warnings and Precautions ( 5.3 )] Hypersensitivity Reactions [see Warnings and Precautions ( 5.4 )] Gastrointestinal Adverse Reactions [see Warnings and Precautions ( 5.5 )] Secondary Malignancies [see Warnings and Precautions ( 5.6 )] Most common (≥20%) adverse reactions or laboratory abnormalities are thrombocytopenia, f …

Do not use if

HEPZATO and the HEPZATO KIT are contraindicated in patients with: Active intracranial metastases or brain lesions with a propensity to bleed Liver failure, portal hypertension, or known varices at risk for bleeding Surgery or medical treatment of the liver in the previous 4 weeks Uncorrectable coagulopathy Inability to safely undergo general anesthesia, including active cardiac conditions including, but not limited to, unstable coronary syndromes (unstable or severe angina or myocardial infarcti …

Warnings

Hypersensitivity reactions, including anaphylaxis, have occurred in patients who received an intravenous (IV) formulation of melphalan. Immediately terminate hepatic arterial melphalan infusion for hypersensitivity reactions and administer supportive care. ( 5.4 ) Gastrointestinal disturbances such as nausea and vomiting, abdominal pain and diarrhea are common. ( 5.5 ) Carcinogenic/Mutagenic effects: Secondary malignancies, including acute nonlymphocytic leukemia, myeloproliferative syndrome, and carcinoma, have been reported in patients with cancer treated with alkylating drugs (including melphalan). Melphalan has been shown to cause chromatid or chromosome damage in humans. …

Pregnancy & breastfeeding

8.1 Pregnancy Risk Summary Based on animal studies and its mechanism of action, melphalan can cause fetal harm when administered to a pregnant woman, including teratogenicity and/or embryo-fetal lethality [see Clinical Pharmacology ( 12.1 ) ]. Melphalan is a genotoxic drug and can cause chromatid or chromosome damage in humans [see Nonclinical Toxicology ( 13.1 ) ]. …

Storage

HEPZATO for injection and its associated diluents including 0.9% sodium chloride must be stored at controlled room temperature 20°C to 25°C (68°F to 77°F). …

General information only — not dosing advice. Always follow the leaflet in your pack and your doctor or pharmacist.

Check your pack of Marc-Blast Lyophilized Powder

Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.

3 free checks left today · no signup Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Marc-Blast Lyophilized Powder

What is in Marc-Blast Lyophilized Powder?

Marc-Blast Lyophilized Powder contains Trafermin (7000 IU/Vial), as powder, according to its NAFDAC registration record.

Is Marc-Blast Lyophilized Powder registered with NAFDAC?

Yes. Marc-Blast Lyophilized Powder is listed on the NAFDAC register under registration number A6-100130, and its registration is active as of 5 November 2026.

Has Marc-Blast Lyophilized Powder been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Marc-Blast Lyophilized Powder in our automatically synced alert list.

How can I check that my pack of Marc-Blast Lyophilized Powder is genuine?

Run a free authenticity scan with the NAFDAC number A6-100130, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

What is Marc-Blast Lyophilized Powder used for?

HEPZATO for injection, as a component of the HEPZATO KIT, is indicated as a liver-directed treatment for adult patients with uveal melanoma with unresectable hepatic metastases affecting less than 50% of the liver and no extrahepatic disease or extrahepatic disease limited to the bone, lymph nodes, subcutaneous tissues, or lung that is amenable to resection or radiation. … (Summarised from the official U.S. FDA label for Marc-Blast Lyophilized Powder. Always follow your doctor or pharmacist.)

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