NDC product
Minoxidil For Women
NDC 69113-502 · BosleyMD
Key facts
| Product NDC | 69113-502 |
|---|---|
| Proprietary name | Minoxidil For Women |
| Nonproprietary name | Minoxidil |
| Substances | MINOXIDIL |
| Dosage form | AEROSOL, FOAM |
| Route | TOPICAL |
| Labeler | BosleyMD |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA208092 |
| Pharmacologic classes | Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC] |
| Marketing start | Aug 29, 2025 |
| 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: