NDC product
Venlafaxine Hydrochloride
NDC 58118-3268 · Clinical Solutions Wholesale
Key facts
| Product NDC | 58118-3268 |
|---|---|
| Proprietary name | Venlafaxine Hydrochloride |
| Labeler | Clinical Solutions Wholesale |
| Marketing category | ANDA |
| Application number | ANDA022104 |
| Marketing start | Apr 29, 2010 |
| Marketing end | Jun 21, 2017 |
| Listing certified through | Jun 21, 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: