Quick answers
- What is Dehydrated alcohol used for?
- The FDA-approved label (Dehydrated Alcohol, Ingenus Pharmaceuticals, LLC, July 11, 2025) says: “Dehydrated alcohol injection is indicated to induce controlled cardiac septal infarction to improve exercise capacity in adults with symptomatic hypertrophic obstructive cardiomyopathy who are not candidates for surgical myectomy. …” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
- Does Dehydrated alcohol 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 Dehydrated alcohol?
- No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
- Has Dehydrated alcohol been recalled?
- No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
- Who makes Dehydrated alcohol?
- 1 company lists prescription products of Dehydrated alcohol in the FDA NDC Directory, including Ingenus Pharmaceuticals, LLC.
What Dehydrated alcohol is used for
Quoted from the “Indications and Usage” section of the FDA-approved label.
Dehydrated alcohol injection is indicated to induce controlled cardiac septal infarction to improve exercise capacity in adults with symptomatic hypertrophic obstructive cardiomyopathy who are not candidates for surgical myectomy. …
— FDA label: Dehydrated Alcohol, Ingenus Pharmaceuticals, LLC, effective July 11, 2025. 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, solution |
|---|---|
| Route | Percutaneous |
| Prescription products | 1 in the FDA NDC Directory |
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.
- Ingenus Pharmaceuticals, LLC1 product
FDA approval history
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
Generic approvals (1)
- ANDA219569Ingenus Pharms LLC · July 9, 2025
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) | 2048982 |
|---|---|
| SPL set ID of the quoted label | 1d5ec6f9-d58f-4651-a4a1-93fec13fd438 |
| FDA labels (SPL) | 1 |
| FDA applications | 1 ANDA |
| Active ingredients (FDA) | DEHYDRATED ALCOHOL |
Sources
- FDA-approved label on DailyMed (National Library of Medicine) — Dehydrated Alcohol, Ingenus Pharmaceuticals, LLC, effective July 11, 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 →