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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
Request
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 NDCNDC-11Package
0037-6321-900003763219090 TABLET in 1 BOTTLE (0037-6321-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1d80a11c-6f86-403b-85d4-32ec1924dbe9
  • NADAC price for package 00037632190

    GET /v1/drugs/nadac/00037632190

Use it

Look up 0037-6321 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0037-6321 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
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.