NDC product
Donepezil Hydrochloride
NDC 0093-0739 · Teva Pharmaceuticals USA Inc
Key facts
| Product NDC | 0093-0739 |
|---|---|
| Proprietary name | Donepezil Hydrochloride |
| Labeler | Teva Pharmaceuticals USA Inc |
| Marketing category | ANDA |
| Application number | ANDA090425 |
| Marketing start | May 31, 2011 |
| Marketing end | Jul 31, 2015 |
| Listing certified through | Jul 31, 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: