NDC product
Mometasone Furoate
NDC 0168-0272 · E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
Key facts
| Product NDC | 0168-0272 |
|---|---|
| Proprietary name | Mometasone Furoate |
| Labeler | E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. |
| Marketing category | ANDA |
| Application number | ANDA075919 |
| Marketing start | Nov 29, 2007 |
| Marketing end | Nov 30, 2017 |
| Listing certified through | Nov 30, 2017 |
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: