adverse reactions
ADVERSE REACTIONS An occasional patient may experience gastrointestinal disturbance or a generalized skin rash. Microscopic and rarely gross hematuria have been described.
Methenamine Mandelate
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
- Methenamine Mandelate
- Generic name
- METHENAMINE MANDELATE
- Manufacturer
- Oncora Pharma, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- d4b79e41-eb29-4d30-aa8f-e964c16bf002
- SPL ID
- 4fa726e6-84de-0f28-e063-6294a90aafe9
- Version
- 1
- Effective date
- 2026-04-17
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:36:03
| 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 |
|---|---|---|---|
| brand name | Methenamine Mandelate | openfda.brand_name | |
| generic name | METHENAMINE MANDELATE | openfda.generic_name | |
| manufacturer name | Oncora Pharma, LLC | openfda.manufacturer_name | |
| ndc | package | 85477-115-16 | openfda.package_ndc |
| ndc | product | 85477-115 | openfda.product_ndc |
| ndc11 | package | 85477011516 | derived:openfda.package_ndc |
| rxcui | 2741045 | openfda.rxcui | |
| spl id | 4fa726e6-84de-0f28-e063-6294a90aafe9 | id | |
| spl set id | d4b79e41-eb29-4d30-aa8f-e964c16bf002 | set_id | |
| unii | 695N30CINR | openfda.unii |
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.