NDC product
LIQUID · Humco Holding Group, Inc.
NDC 0395-2775 · Humco Holding Group, Inc.
Key facts
| Product NDC | 0395-2775 |
|---|---|
| Nonproprietary name | Iodine and potassium iodide |
| Substances | IODINE, POTASSIUM IODIDE |
| Dosage form | LIQUID |
| Labeler | Humco Holding Group, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | DRUG FOR FURTHER PROCESSING |
| Marketing start | Jan 1, 2008 |
| Listing certified through | Dec 31, 2026 |
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: