NDC product
METAVEX
NDC 85477-503 · Oncora Pharma, LLC
Key facts
| Product NDC | 85477-503 |
|---|---|
| Proprietary name | METAVEX |
| Nonproprietary name | METAVEX |
| Substances | CHOLECALCIFEROL, FOLIC ACID, BLUE AGAVE INULIN (AGAVE TEQUILANA), ELM, ALOE FEROX LEAF, RHAMNUS CATHARTICA BARK |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Oncora Pharma, LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Pharmacologic classes | Vitamin D [CS], Vitamin D [EPC] |
| Marketing start | Jan 1, 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: