NDC product
HYDROCORTISONE BUTYRATE
NDC 68682-392 · Oceanside Pharmaceuticals
Key facts
| Product NDC | 68682-392 |
|---|---|
| Proprietary name | HYDROCORTISONE BUTYRATE |
| Labeler | Oceanside Pharmaceuticals |
| Marketing category | NDA AUTHORIZED GENERIC |
| Application number | NDA022076 |
| Marketing start | Jun 8, 2018 |
| Marketing end | Sep 30, 2025 |
| Listing certified through | Sep 30, 2025 |
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: