NDC product
Hydrochlorothiazide
NDC 72162-1356 · Bryant Ranch Prepack
Key facts
| Product NDC | 72162-1356 |
|---|---|
| Proprietary name | Hydrochlorothiazide |
| Labeler | Bryant Ranch Prepack |
| Marketing category | ANDA |
| Application number | ANDA040412 |
| Marketing start | Mar 29, 2002 |
| Marketing end | May 11, 2026 |
| Listing certified through | May 11, 2026 |
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: