Medical emergency?Emergency? Call 911. Nearest emergency roomsNearest ERs

Prescription medicine

Sacrosidase

Drug class: Sucrose-specific Enzyme

The FDA’s “Established Pharmacologic Class”: the group of medicines that work in a similar way.

Official FDA data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the drug label, the NDC Directory, Drugs@FDA, recall reports and the drug shortage list. Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

What is Sacrosidase used for?
The FDA-approved label (Sucraid, QOL Medical, LLC, December 29, 2025) says: “Sucraid ® (sacrosidase) Oral Solution is indicated for the treatment of sucrase deficiency, which is part of congenital sucrase-isomaltase deficiency (CSID), in adult and pediatric patients 5 months of age and older.” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Does Sacrosidase 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 Sacrosidase?
No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
Has Sacrosidase been recalled?
No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
Who makes Sacrosidase?
1 company lists prescription products of Sacrosidase in the FDA NDC Directory, including QOL Medical, LLC.

What Sacrosidase is used for

Quoted from the “Indications and Usage” section of the FDA-approved label.

Sucraid ® (sacrosidase) Oral Solution is indicated for the treatment of sucrase deficiency, which is part of congenital sucrase-isomaltase deficiency (CSID), in adult and pediatric patients 5 months of age and older.

— FDA label: Sucraid, QOL Medical, LLC, effective December 29, 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 formsSolution
RouteOral
Prescription products1 in the FDA NDC Directory
Brand namesSucraid

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.
Brand and biologic applications
ApplicationSponsorApprovedLater changes approved
BLA020772
SUCRAID
Qol MedclApril 9, 1998 15, latest August 2, 2024
2024: Labeling · 2024: Labeling · 2022: Manufacturing (CMC)

Shortage status

The FDA drug shortage list does not show these products.

FDA Drug Shortages database →

Recalls

No recall linked to these products (by their NDC code) appears in the FDA enforcement reports.

Official identifiers

RxCUI (RxNorm)213337, 312872
SPL set ID of the quoted labeld613bb7f-c3f4-462e-81a2-da2347cc4b6b
FDA labels (SPL)1
FDA applicationsBLA020772
Active ingredients (FDA)SACROSIDASE

Sources

  1. FDA-approved label on DailyMed (National Library of Medicine) — Sucraid, QOL Medical, LLC, effective December 29, 2025; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. 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 →

Report an error → · Information for medicine makers