NDC product
VUSION
NDC 0378-8222 · Mylan Pharmaceuticals Inc.
Key facts
| Product NDC | 0378-8222 |
|---|---|
| Proprietary name | VUSION |
| Nonproprietary name | miconazole nitrate, zinc oxide, white petrolatum |
| Substances | MICONAZOLE NITRATE, ZINC OXIDE, PETROLATUM |
| Dosage form | OINTMENT |
| Route | TOPICAL |
| Labeler | Mylan Pharmaceuticals Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA AUTHORIZED GENERIC |
| Application number | NDA021026 |
| Pharmacologic classes | Azole Antifungal [EPC], Azoles [CS] |
| Marketing start | Nov 6, 2018 |
| Marketing end | Dec 31, 2026 |
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