NDC product
Guiatuss
NDC 0182-0259 · Goldline Laboratories, Inc.
Key facts
| Product NDC | 0182-0259 |
|---|---|
| Proprietary name | Guiatuss |
| Labeler | Goldline Laboratories, Inc. |
| Marketing category | OTC MONOGRAPH FINAL |
| Application number | part341 |
| Marketing start | Sep 30, 1990 |
| Marketing end | Mar 28, 2000 |
| Listing certified through | Mar 28, 2000 |
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: