NDC product
ACD Solution Modified
NDC 51808-201 · AnazaoHealth Corporation
Key facts
| Product NDC | 51808-201 |
|---|---|
| Proprietary name | ACD Solution Modified |
| Labeler | AnazaoHealth Corporation |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing start | May 23, 2012 |
| Listing certified through | Dec 31, 2017 |
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: