NDC product
Hydrocortisone Acetate
NDC 0904-7340 · Major Pharmaceuticals
Key facts
| Product NDC | 0904-7340 |
|---|---|
| Proprietary name | Hydrocortisone Acetate |
| Nonproprietary name | Hydrocortisone Acetate |
| Substances | HYDROCORTISONE ACETATE |
| Dosage form | SUPPOSITORY |
| Route | RECTAL |
| Labeler | Major Pharmaceuticals |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Pharmacologic classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
| Marketing start | Apr 5, 2024 |
| Marketing end | Feb 28, 2027 |
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