NDC product
Ascorbic Acid
NDC 0517-5050 · American Regent, Inc.
Key facts
| Product NDC | 0517-5050 |
|---|---|
| Proprietary name | Ascorbic Acid |
| Labeler | American Regent, Inc. |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing start | Dec 15, 1989 |
| Marketing end | Mar 28, 2008 |
| Listing certified through | Mar 28, 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: