Quick answers
- What is Coral snake (micrurus fulvius) immune globulin antivenin (equine) used for?
- The FDA-approved label (North American Coral Snake Antivenin (Equine), Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc., November 22, 2022) says: “North American Coral Snake Antivenin (Equine) is indicated only for the treatment of envenomation caused by bites of North American coral snakes - Micrurus (including the eastern and Texas varieties). North American Coral Snake Antivenin (Equine) is a horse-derived antivenin indicated for the treatment of envenomation caused by North American coral snakes - Micrurus.” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
- Does Coral snake (micrurus fulvius) immune globulin antivenin (equine) have a boxed warning?
- No. None of the 1 FDA labels we found for this medicine has a boxed warning.
- Is there a shortage of Coral snake (micrurus fulvius) immune globulin antivenin (equine)?
- No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
- Has Coral snake (micrurus fulvius) immune globulin antivenin (equine) been recalled?
- No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
- Who makes Coral snake (micrurus fulvius) immune globulin antivenin (equine)?
- 1 company lists prescription products of Coral snake (micrurus fulvius) immune globulin antivenin (equine) in the FDA NDC Directory, including Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc..
What Coral snake (micrurus fulvius) immune globulin antivenin (equine) is used for
Quoted from the “Indications and Usage” section of the FDA-approved label.
North American Coral Snake Antivenin (Equine) is indicated only for the treatment of envenomation caused by bites of North American coral snakes - Micrurus (including the eastern and Texas varieties). North American Coral Snake Antivenin (Equine) is a horse-derived antivenin indicated for the treatment of envenomation caused by North American coral snakes - Micrurus.
— FDA label: North American Coral Snake Antivenin (Equine), Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc., effective November 22, 2022. Read the full label on DailyMed →
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.
Forms and how it is given
| Dosage forms | Injection, powder, for solution |
|---|---|
| Route | Intravenous |
| Prescription products | 1 in the FDA NDC Directory |
| Brand names | North American Coral Snake Antivenin (Equine) |
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.
FDA approval history
- BLA: Biologics License Application: how a biologic medicine (made from living cells) is approved.
| Application | Sponsor | Approved | Later changes approved |
|---|---|---|---|
| BLA101099 | — | Date not on file | — |
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) | 1858981 |
|---|---|
| SPL set ID of the quoted label | 6d0f94b4-82ca-37c7-edb0-4f0702cf6c8d |
| FDA labels (SPL) | 1 |
| FDA applications | BLA101099 |
| Active ingredients (FDA) | CORAL SNAKE (MICRURUS FULVIUS) IMMUNE GLOBULIN ANTIVENIN (EQUINE) |
Sources
- FDA-approved label on DailyMed (National Library of Medicine) — North American Coral Snake Antivenin (Equine), Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc., effective November 22, 2022; 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 →