NDC product
Olivita Extra Strength Minoxidil
NDC 87695-008 · Olivita Beauty Inc
Key facts
| Product NDC | 87695-008 |
|---|---|
| Proprietary name | Olivita Extra Strength Minoxidil |
| Nonproprietary name | MINOXIDIL |
| Substances | MINOXIDIL |
| Dosage form | SOLUTION |
| Route | TOPICAL |
| Labeler | Olivita Beauty Inc |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA076239 |
| Pharmacologic classes | Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC] |
| Marketing start | Aug 6, 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: