NDC product
Potassium Chloride
NDC 0603-1554 · Endo USA, Inc.
Key facts
| Product NDC | 0603-1554 |
|---|---|
| Proprietary name | Potassium Chloride |
| Nonproprietary name | Potassium Chloride |
| Substances | POTASSIUM CHLORIDE |
| Dosage form | POWDER, FOR SOLUTION |
| Route | ORAL |
| Labeler | Endo USA, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Application number | NDA208019 |
| Marketing start | Sep 18, 2015 |
| 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: