URELLE .12 mg/1
hyoscyamine sulfate, methenamine, methylene blue, phenyl salicylate, and sodium phosphate, monobasic, monohydrate · TABLET · Viatris Specialty LLC
URELLE is a tablet containing hyoscyamine sulfate, methenamine, methylene blue, phenyl salicylate, and sodium phosphate, monobasic, monohydrate at .12 mg/1, taken oral. Manufactured by Viatris Specialty LLC.
Key Facts
- Brand Name
- URELLE
- Generic Name
- hyoscyamine sulfate, methenamine, methylene blue, phenyl salicylate, and sodium phosphate, monobasic, monohydrate
- NDC Code (Product)
0037-6321- Manufacturer
- Viatris Specialty LLC
- Strength
- .12 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Marketing Start
- 01/12/2015
Recall History
No Recall HistoryFrequently Asked Questions
What is URELLE used for?
URELLE contains hyoscyamine sulfate, methenamine, methylene blue, phenyl salicylate, and sodium phosphate, monobasic, monohydrate. It is a tablet taken oral. Consult your doctor for specific uses.
Is URELLE a controlled substance?
URELLE is not classified as a controlled substance by the DEA.
What is the generic name for URELLE?
The generic name for URELLE is hyoscyamine sulfate, methenamine, methylene blue, phenyl salicylate, and sodium phosphate, monobasic, monohydrate. There are no other listed brand versions of hyoscyamine sulfate, methenamine, methylene blue, phenyl salicylate, and sodium phosphate, monobasic, monohydrate.
What is the NDC code for URELLE .12 mg/1?
The NDC (National Drug Code) for URELLE .12 mg/1 is 0037-6321, listed by Viatris Specialty LLC.
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)