NDC product
Minoxidil Topical Solution
NDC 87399-002 · Growth Essence LLC
Key facts
| Product NDC | 87399-002 |
|---|---|
| Proprietary name | Minoxidil Topical Solution |
| Nonproprietary name | Minoxidil Topical Solution |
| Substances | MINOXIDIL |
| Dosage form | LIQUID |
| Route | TOPICAL |
| Labeler | Growth Essence LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | 505G(a)(3) |
| Pharmacologic classes | Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC] |
| Marketing start | May 16, 2026 |
| 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: