NDC product
Benazepril Hydrochloride and Hydrochlorothiazide
NDC 0185-0204 · Eon Labs, Inc.
Key facts
| Product NDC | 0185-0204 |
|---|---|
| Proprietary name | Benazepril Hydrochloride and Hydrochlorothiazide |
| Labeler | Eon Labs, Inc. |
| Marketing category | ANDA |
| Application number | ANDA076631 |
| Marketing start | Feb 11, 2004 |
| Marketing end | Jan 30, 2018 |
| Listing certified through | Jan 30, 2018 |
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: