NDC product
Emvita 7
NDC 66343-094 · RUBIMED AG
Key facts
| Product NDC | 66343-094 |
|---|---|
| Proprietary name | Emvita 7 |
| Nonproprietary name | Anacard occ, Glandula sup, Lachesis mutus, Lycopodium, Phosphorus |
| Substances | ANACARDIUM OCCIDENTALE FRUIT, SUS SCROFA ADRENAL GLAND, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, PHOSPHORUS |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | RUBIMED AG |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | Dec 21, 2022 |
| Listing certified through | 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 · Source date: