NDC product
URELLE
NDC 0037-6321 · Viatris Specialty LLC
Key facts
| Product NDC | 0037-6321 |
|---|---|
| Proprietary name | URELLE |
| Nonproprietary name | hyoscyamine sulfate, methenamine, methylene blue, phenyl salicylate, and sodium phosphate, monobasic, monohydrate |
| Substances | HYOSCYAMINE SULFATE, METHENAMINE, METHYLENE BLUE, PHENYL SALICYLATE, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Viatris Specialty LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Pharmacologic classes | Oxidation-Reduction Activity [MoA], Oxidation-Reduction Agent [EPC] |
| Marketing start | Jan 12, 2015 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: