UROGESIC BLUE
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
- UROGESIC BLUE
- Generic name
- METHENAMINE, SODIUM PHOSPHATE, MONOBASIC, METHYLENE BLUE, AND HYOSCYAMINE SULFATE
- Manufacturer
- EDWARDS PHARMACEUTICALS, INC.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- d820e42d-ad2b-4e11-907b-a94d698ca285
- SPL ID
- 3c4170bc-d3bf-74df-e063-6294a90ad846
- Version
- 4
- Effective date
- 2025-08-13
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:55:55
| 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 | UROGESIC BLUE | openfda.brand_name | |
| generic name | METHENAMINE, SODIUM PHOSPHATE, MONOBASIC, METHYLENE BLUE, AND HYOSCYAMINE SULFATE | openfda.generic_name | |
| manufacturer name | EDWARDS PHARMACEUTICALS, INC. | openfda.manufacturer_name | |
| ndc | package | 0485-0151-30 | openfda.package_ndc |
| ndc | product | 0485-0151 | openfda.product_ndc |
| ndc11 | package | 00485015130 | derived:openfda.package_ndc |
| rxcui | 1050325 | openfda.rxcui | |
| rxcui | 1251290 | openfda.rxcui | |
| spl id | 3c4170bc-d3bf-74df-e063-6294a90ad846 | id | |
| spl set id | d820e42d-ad2b-4e11-907b-a94d698ca285 | set_id | |
| unii | T42P99266K | openfda.unii | |
| unii | F2R8V82B84 | openfda.unii | |
| unii | J50OIX95QV | openfda.unii | |
| unii | 3980JIH2SW | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS Do not exceed recommended dosage. If rapid pulse, dizziness, or blurring of vision occurs discontinue use immediately.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS Cardiovascular – rapid pulse, flushing Central Nervous System – blurred vision, dizziness Respiratory – shortness of breath or troubled breathing Genitourinary – difficulty micturition, acute urinary retention Gastrointestinal – dry mouth, nausea/vomiting
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.