NDC product
Priscoline hydrochloride
NDC 0083-6733 · Novartis Pharmaceuticals Corporation
Key facts
| Product NDC | 0083-6733 |
|---|---|
| Proprietary name | Priscoline hydrochloride |
| Labeler | Novartis Pharmaceuticals Corporation |
| Marketing category | NDA |
| Application number | NDA006403 |
| Marketing start | Mar 17, 1948 |
| Marketing end | Aug 18, 2008 |
| Listing certified through | Aug 18, 2008 |
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: