NDC product
DONEPEZIL HYDROCHLORIDE
NDC 63187-401 · Proficient Rx LP
Key facts
| Product NDC | 63187-401 |
|---|---|
| Proprietary name | DONEPEZIL HYDROCHLORIDE |
| Labeler | Proficient Rx LP |
| Marketing category | ANDA |
| Application number | ANDA090768 |
| Marketing start | May 29, 2011 |
| Marketing end | Nov 30, 2022 |
| Listing certified through | Nov 30, 2022 |
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: