NDC product
Olopatadine Hydrochloride
NDC 61314-320 · Sandoz Inc
Key facts
| Product NDC | 61314-320 |
|---|---|
| Proprietary name | Olopatadine Hydrochloride |
| Labeler | Sandoz Inc |
| Marketing category | NDA AUTHORIZED GENERIC |
| Application number | NDA021861 |
| Marketing start | Apr 1, 2015 |
| Marketing end | Feb 29, 2024 |
| Listing certified through | Feb 29, 2024 |
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: