NDC product
Azelastine Hydrochloride
NDC 0832-0290 · Upsher-Smith Laboratories, Inc.
Key facts
| Product NDC | 0832-0290 |
|---|---|
| Proprietary name | Azelastine Hydrochloride |
| Labeler | Upsher-Smith Laboratories, Inc. |
| Marketing category | ANDA |
| Application number | ANDA202609 |
| Marketing start | Mar 17, 2017 |
| Marketing end | Mar 17, 2017 |
| Listing certified through | Mar 17, 2017 |
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: