NDC product
CV HP
NDC 44911-0196 · ENERGIQUE, INC.
Key facts
| Product NDC | 44911-0196 |
|---|---|
| Proprietary name | CV |
| Nonproprietary name | Adonis vernalis, Lachesis mutus, Lycopus virginicus, Valeriana officinalis, Aurum metallicum, Cactus grandiflorus, Digitalis purpurea, Natrum muriaticum, Phosphorus, Pulsatilla (pratensis) |
| Substances | ADONIS VERNALIS WHOLE, LACHESIS MUTA VENOM, LYCOPUS VIRGINICUS WHOLE, VALERIAN, GOLD, SELENICEREUS GRANDIFLORUS STEM, DIGITALIS, SODIUM CHLORIDE, PHOSPHORUS, PULSATILLA PRATENSIS |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | ENERGIQUE, INC. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC] |
| Marketing start | Jul 9, 2015 |
| 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: