NDC product
Lisinopril and Hydrochlorothiazide
NDC 16571-793 · Rising Pharma Holdings, Inc.
Key facts
| Product NDC | 16571-793 |
|---|---|
| Proprietary name | Lisinopril and Hydrochlorothiazide |
| Labeler | Rising Pharma Holdings, Inc. |
| Marketing category | ANDA |
| Application number | ANDA077606 |
| Marketing start | Mar 14, 2006 |
| Marketing end | Mar 15, 2006 |
| Listing certified through | Mar 15, 2006 |
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: