NDC product
Tucks Hemorrhoidal
NDC 30014-100 · Johnson & Johnson Consumer Inc.
Key facts
| Product NDC | 30014-100 |
|---|---|
| Proprietary name | Tucks Hemorrhoidal |
| Labeler | Johnson & Johnson Consumer Inc. |
| Marketing category | OTC MONOGRAPH FINAL |
| Application number | part346 |
| Marketing start | Jul 30, 2012 |
| Marketing end | Jul 15, 2016 |
| Listing certified through | Jul 15, 2016 |
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: