Sucraid
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Sucraid
- Generic name
- SACROSIDASE
- Manufacturer
- QOL Medical, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- d613bb7f-c3f4-462e-81a2-da2347cc4b6b
- SPL ID
- 4719ec33-5660-444a-e063-6294a90ab40c
- Version
- 21
- Effective date
- 2025-12-29
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:18:54
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | BLA | 020772 | derived:openfda.application_number |
| application number | BLA020772 | openfda.application_number | |
| brand name | Sucraid | openfda.brand_name | |
| generic name | SACROSIDASE | openfda.generic_name | |
| manufacturer name | QOL Medical, LLC | openfda.manufacturer_name | |
| ndc | package | 67871-111-05 | openfda.package_ndc |
| ndc | package | 67871-111-07 | openfda.package_ndc |
| ndc | package | 67871-111-01 | openfda.package_ndc |
| ndc | package | 67871-111-04 | openfda.package_ndc |
| ndc | package | 67871-111-06 | openfda.package_ndc |
| ndc | product | 67871-111 | openfda.product_ndc |
| ndc11 | package | 67871011106 | derived:openfda.package_ndc |
| ndc11 | package | 67871011101 | derived:openfda.package_ndc |
| ndc11 | package | 67871011107 | derived:openfda.package_ndc |
| ndc11 | package | 67871011104 | derived:openfda.package_ndc |
| ndc11 | package | 67871011105 | derived:openfda.package_ndc |
| rxcui | 213337 | openfda.rxcui | |
| rxcui | 312872 | openfda.rxcui | |
| spl id | 4719ec33-5660-444a-e063-6294a90ab40c | id | |
| spl set id | d613bb7f-c3f4-462e-81a2-da2347cc4b6b | set_id | |
| unii | 8A7F670F2Y | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS Severe Hypersensitivity Reactions Severe hypersensitivity reactions, including wheezing, rash, and pruritis, have been reported with administration of Sucraid. Sucraid contains papain, which is associated with hypersensitivity reactions (see DESCRIPTION). A pediatric patient in the clinical trials experienced a hypersensitivity reaction of severe wheezing that required hospitalization. Postmarketing cases of cutaneous hypersensitivity reactions have also been reported. Instruct patients or caregivers to stop Sucraid and seek medical attention if symptoms suggestive of a hypersensitivity reaction occur. Sucraid is contraindicated in patients who have had a known hypersensitivity reaction (see CONTRAINDICATIONS).
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS The following adverse reactions associated with the use of sacrosidase were identified in clinical studies or postmarketing reports. Because some of these reactions were reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. In clinical studies of up to 54 months duration, a total of 52 patients were treated with Sucraid. The reported adverse reactions (number of patients) were as follows: abdominal pain (4), vomiting (3), nausea (2), diarrhea (2), constipation (2), insomnia (1), headache (1), nervousness (1), and dehydration (1). Hypersensitivity reactions (wheezing, rash, and pruritis) have been reported (see WARNINGS).
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.