NDC product
DRY-CID
NDC 81943-601 · Aqua Medica, S.A. de C.V.
Key facts
| Product NDC | 81943-601 |
|---|---|
| Proprietary name | DRY-CID |
| Nonproprietary name | Dry Concentrate for Hemodialysis |
| Substances | POTASSIUM CHLORATE |
| Dosage form | POWDER, FOR SOLUTION |
| Route | HEMODIALYSIS |
| Labeler | Aqua Medica, S.A. de C.V. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing start | Mar 30, 2023 |
| 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: