NDC product
SUFLAVE
NDC 24338-550 · Azurity Pharmaceuticals, Inc.
Key facts
| Product NDC | 24338-550 |
|---|---|
| Proprietary name | SUFLAVE |
| Nonproprietary name | polyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution |
| Dosage form | KIT |
| Labeler | Azurity Pharmaceuticals, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Application number | NDA215344 |
| Marketing start | Apr 1, 2026 |
| 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: