Quick answers
- What is Succimer used for?
- The FDA-approved label (Chemet, Recordati Rare Diseases, Inc., July 10, 2025) says: “CHEMET is indicated for the treatment of lead poisoning in pediatric patients aged 1 year and older with blood lead levels above 45 mcg/dL. CHEMET is a lead chelator indicated for the treatment of lead poisoning in pediatric patients aged 1 year and older with blood lead levels above 45 mcg/dL. Limitations of Use CHEMET is not indicated for prophylaxis of lead poisoning in a lead-containing environment. …” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
- Does Succimer have a boxed warning?
- No. None of the 2 FDA labels we found for this medicine has a boxed warning.
- Is there a shortage of Succimer?
- No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
- Has Succimer been recalled?
- No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
- Who makes Succimer?
- 2 companies list prescription products of Succimer in the FDA NDC Directory, including Recordati Rare Diseases, Inc. and Theragnostics Inc.
What Succimer is used for
Quoted from the “Indications and Usage” section of the FDA-approved label.
CHEMET is indicated for the treatment of lead poisoning in pediatric patients aged 1 year and older with blood lead levels above 45 mcg/dL. CHEMET is a lead chelator indicated for the treatment of lead poisoning in pediatric patients aged 1 year and older with blood lead levels above 45 mcg/dL. Limitations of Use CHEMET is not indicated for prophylaxis of lead poisoning in a lead-containing environment. …
— FDA label: Chemet, Recordati Rare Diseases, Inc., effective July 10, 2025. Read the full label on DailyMed →
The FDA has 2 labels for products of this medicine (different makers and forms); uses can differ between them. Check the label that comes with your own medicine.
This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Boxed warning
A boxed warning (“black box”) is the FDA’s strongest warning on a drug label, for serious or life-threatening risks.
The label quoted above has no boxed warning.
0 of 2 FDA labels for this medicine have a boxed warning.
Forms and how it is given
| Dosage forms | Capsule · Injection, powder, lyophilized, for solution |
|---|---|
| Route | Oral · Intravenous |
| Prescription products | 2 in the FDA NDC Directory |
| Brand names | Chemet, Nephroscan |
Companies that list this medicine
Labelers in the FDA NDC Directory: the company named on the package (maker or distributor), with the number of prescription products.
- Recordati Rare Diseases, Inc.1 product
- Theragnostics Inc1 product
FDA approval history
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
Shortage status
The FDA drug shortage list does not show these products.
Recalls
No recall linked to these products (by their NDC code) appears in the FDA enforcement reports.
Official identifiers
| RxCUI (RxNorm) | 198227, 207949 |
|---|---|
| SPL set ID of the quoted label | 62035612-9505-3a3f-1ac8-e2dbd711d24e |
| FDA labels (SPL) | 2 |
| FDA applications | NDA019998, NDA214993 |
| Active ingredients (FDA) | SUCCIMER |
Sources
- FDA-approved label on DailyMed (National Library of Medicine) — Chemet, Recordati Rare Diseases, Inc., effective July 10, 2025; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- Drug shortages (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
openFDA data is provided by the FDA as is; it may be incomplete. Always rely on the label that comes with your medicine. FDA Enforcement Report search →