URELLE
NDC 0037-6321, hyoscyamine sulfate, methenamine, methylene blue, phenyl salicylate, and sodium phosphate, monobasic, monohydrate, tablet, from Viatris Specialty LLC.
- Product NDC
- 0037-6321
- Status
- Listed
- Labeler
- Viatris Specialty LLC
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0037-6321 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- HYOSCYAMINE SULFATE.12 mg/1
- METHENAMINE81 mg/1
- METHYLENE BLUE10.8 mg/1
- PHENYL SALICYLATE32.4 mg/1
- SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE40.8 mg/1
Pharmacologic classes
Oxidation-Reduction Activity [MoA]; Oxidation-Reduction Agent [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0037-6321-90 | 00037632190 | 90 TABLET in 1 BOTTLE (0037-6321-90) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/1d80a11c-6f86-403b-85d4-32ec1924dbe9NADAC price for package 00037632190
GET /v1/drugs/nadac/00037632190
Use it
Look up 0037-6321 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0037-6321 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0037-6321. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.