NDC product
Maximum Strength Hydrocortisone
NDC 24286-1560 · DLC Laboratories, Inc
Key facts
| Product NDC | 24286-1560 |
|---|---|
| Proprietary name | Maximum Strength Hydrocortisone |
| Nonproprietary name | HYDROCORTISONE |
| Substances | HYDROCORTISONE |
| Dosage form | OINTMENT |
| Route | TOPICAL |
| Labeler | DLC Laboratories, Inc |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M017 |
| Pharmacologic classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
| Marketing start | Mar 22, 2013 |
| Listing certified through | Dec 31, 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 · Source date: