NDC product
Moisturel
NDC 0093-3204 · Teva Pharmaceuticals USA, Inc.
Key facts
| Product NDC | 0093-3204 |
|---|---|
| Proprietary name | Moisturel |
| Labeler | Teva Pharmaceuticals USA, Inc. |
| Marketing category | OTC MONOGRAPH FINAL |
| Application number | part347 |
| Marketing start | Nov 12, 2018 |
| Marketing end | Aug 25, 2023 |
| Listing certified through | Aug 25, 2023 |
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: