NDC product
Donepezil Hydrochloride 10 mg
NDC 16714-385 · NorthStar RxLLC
Key facts
| Product NDC | 16714-385 |
|---|---|
| Proprietary name | Donepezil Hydrochloride |
| Labeler | NorthStar RxLLC |
| Marketing category | ANDA |
| Application number | ANDA201724 |
| Marketing start | Feb 19, 2013 |
| Marketing end | May 25, 2015 |
| Listing certified through | May 25, 2015 |
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: