NDC product
Fosinopril Sodium and Hydrochlorothiazide
NDC 23155-061 · Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Key facts
| Product NDC | 23155-061 |
|---|---|
| Proprietary name | Fosinopril Sodium and Hydrochlorothiazide |
| Labeler | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. |
| Marketing category | ANDA |
| Application number | ANDA079025 |
| Marketing start | Nov 15, 2011 |
| Marketing end | Aug 11, 2020 |
| Listing certified through | Aug 11, 2020 |
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: