NDC product
UROGESIC BLUE
NDC 0485-0151 · EDWARDS PHARMACEUTICALS, INC.
Key facts
| Product NDC | 0485-0151 |
|---|---|
| Proprietary name | UROGESIC BLUE |
| Nonproprietary name | METHENAMINE, SODIUM PHOSPHATE, MONOBASIC, METHYLENE BLUE, and HYOSCYAMINE SULFATE |
| Substances | METHENAMINE, SODIUM PHOSPHATE, MONOBASIC, METHYLENE BLUE, HYOSCYAMINE SULFATE |
| Dosage form | TABLET, COATED |
| Route | ORAL |
| Labeler | EDWARDS PHARMACEUTICALS, INC. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Pharmacologic classes | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Oxidation-Reduction Activity [MoA], Oxidation-Reduction Agent [EPC] |
| Marketing start | Nov 19, 2010 |
| 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: