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Medicare Part D spending · FDA facts · help paying

Sucraid (sacrosidase): what Medicare Part D spends and the dated federal facts we hold

CMS's Medicare Part D spending dataset reports gross spending on Sucraid of $107.66 million in 2024, across 8,121 claims and 2,168 beneficiaries.

Assistance programs: 0CMS Part D spending, data year 2024Drugs@FDA, read November 7, 2026
0programs in our finder list this drug
$107.66 millionMedicare Part D gross spending in 2024, before manufacturer rebates; not a patient price
3federal data layers besides Part D spending hold facts for this drug: FDA application facts, biosimilar status, federal formularies

Medicare Part D spending

CMS's Medicare Part D spending dataset reports gross spending on Sucraid of $107.66 million in 2024, across 8,121 claims and 2,168 beneficiaries. CMS's dataset states spending is gross drug cost and does not reflect manufacturers' rebates or other price concessions. Spending is the total paid by Medicare, plans and beneficiaries for the drug's claims, not what a patient pays.

$37.83 million2020$46.62 million2021$53.13 million2022$77.41 million2023$107.66 million2024Gross spending before rebates, not a patient price
Source: CMS Medicare Part D spending by drug, reported under Sucraid; gross spending before manufacturer rebates.
YearGross spendingClaimsBeneficiariesAverage spending per claim
2024$107.66 million8,1212,168$13,257
2023$77.41 million6,1301,656$12,627
2022$53.13 million4,5511,159$11,674
2021$46.62 million4,053976$11,504
2020$37.83 million3,429798$11,034

Source: CMS Medicare Part D spending by drug (data-year-2024, modified 2026-06-25), read November 7, 2026. CMS dataset page. All manufacturers combined; the figures are a drug-level aggregate of claims and say nothing about a formulary or coverage.

Biosimilar status

  • Sucraid (sacrosidase) is a reference product in the FDA Purple Book (BLA 020772, approved April 9, 1998). The Purple Book lists 0 biosimilars and 0 interchangeable products that name it as their reference product.

This is what the FDA Purple Book lists on the read date. It is a record, not a forecast of when any product will launch or be substituted.

Source: FDA Purple Book (purplebook-2026-10), read November 7, 2026. Purple Book data file.

FDA safety program (REMS)

  • Sucraid (application BLA020772): listed as released, with Elements to Assure Safe Use. Program dated November 20, 2008, last modified December 9, 2010. REMS@FDA program page.

A REMS is a safety program the FDA can require for a drug. Some restrict how it is prescribed or dispensed, for example through certified prescribers or pharmacies. This lists what the FDA's REMS@FDA files tie to the application; it does not say which prescribers or pharmacies take part, or whether a given patient needs the program.

Source: FDA REMS@FDA data files (rems-fda-files-2026-11-07-products-20a9945448dd), read November 7, 2026. REMS@FDA product file.

Rare-disease (orphan) designations

The FDA's orphan drug database lists 1 designation for Sacrosidase, 1 with an approval recorded. A designation is not an approval and not a statement that the drug treats the condition; the status column is the database's own.

DesignatedDesignated useStatusSponsor
December 10, 1993Treatment of congenital sucrase-isomaltase deficiencyDesignated/ApprovedQOL Medical, LLC

Source: FDA Orphan Drug Designations and Approvals database, read November 7, 2026. FDA orphan drug search.

Federal formulary status

VA national formulary

The VA's national formulary files list the ingredient sacrosidase, which covers every maker's product with that ingredient, not only Sucraid. Each row is a VA national drug file entry and its status.

VA entryStatusActive NDCs
SACROSIDASE SOLN,ORALNon-formulary3

Source: VA Pharmacy Benefits Management national formulary (va-formulary-2026-09), read November 7, 2026. VA formulary page.

Where help paying exists

No program in our finder currently lists this drug as open to new patients.

Label changes

The FDA file lists no non-manufacturing label change for these applications since November 11, 2025. The most recent one it lists is dated August 2, 2024 (Labeling).

Source: FDA Drugs@FDA data file, read November 7, 2026. Dates are the FDA action dates; the documents are on FDA's own site. FDA data file. All recent changes across these drugs: label changes feed.

Questions

Does Medicare have a negotiated price for Sucraid?

The CMS negotiated-price file we read does not list Sucraid, so this page shows no negotiated price. A drug appears in that file only when CMS selects it for negotiation, and not being listed says nothing about what it costs a patient.

Is there help paying for Sucraid?

No program in our finder lists this drug yet.

How much does Medicare Part D spend on Sucraid?

CMS's Medicare Part D spending dataset reports gross spending on Sucraid of $107.66 million in 2024, across 8,121 claims and 2,168 beneficiaries. CMS's dataset states spending is gross drug cost and does not reflect manufacturers' rebates or other price concessions. Spending is the total paid by Medicare, plans and beneficiaries for the drug's claims, not what a patient pays.

For developers: this drug as data

One call returns the generic-entry upper bound, label history, recalls, trials, assistance and Part D spending, and where facts exist the FDA safety program (REMS), DEA schedule, orphan designations, safety notices and Medicaid use by state, each with receipts.

Example file: https://omnirx.org/api/v1/dossier/sucraid.json

The licence page sets out what a data licence covers, and the API page documents these files.

Evaluation files with receipts; contract may change; not clinical advice.

Sources and terms. This drug is not in the CMS negotiated-price file, so no price source is used. Program details read from each program's own pages; CMS Medicare Part D spending by drug; TRICARE and VA formulary files; FDA Purple Book; FDA Drugs@FDA and Orange Book data files. Figures are stored with their sources in the OmniRx library (edition 2026-11). Free to cite with attribution. Not medical, legal or financial advice. Report an error through the contact page. Licence the data.