NDC product
Fosinopril Sodium and Hydrochlorothiazide
NDC 15330-233 · Genpharm ULC
Key facts
| Product NDC | 15330-233 |
|---|---|
| Proprietary name | Fosinopril Sodium and Hydrochlorothiazide |
| Labeler | Genpharm ULC |
| Marketing category | ANDA |
| Application number | ANDA077705 |
| Marketing start | Nov 1, 2015 |
| Marketing end | Nov 30, 2015 |
| Listing certified through | Nov 30, 2015 |
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: