NDC product
Moexipril hydrochloride/hydrochlorothiazide
NDC 16252-612 · Cobalt Laboratories
Key facts
| Product NDC | 16252-612 |
|---|---|
| Proprietary name | Moexipril hydrochloride/hydrochlorothiazide |
| Labeler | Cobalt Laboratories |
| Marketing category | NDA |
| Application number | NDA020729 |
| Marketing start | Mar 15, 2007 |
| Marketing end | Mar 31, 2013 |
| Listing certified through | Mar 31, 2013 |
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: