NDC product
Lymphastat F
NDC 44911-0706 · Energique, Inc
Key facts
| Product NDC | 44911-0706 |
|---|---|
| Proprietary name | Lymphastat F |
| Nonproprietary name | Echinacea (Angustifolia), Tabebuia Impetiginosa, Abies Nigra, Borax, Lycopodium Clavatum, Nux Vomica, Phosphorus, Pulsatilla (Vulgaris), Sepia, Thuja Occidentalis, Skatolum, Candida Albicans |
| Substances | ECHINACEA ANGUSTIFOLIA WHOLE, HANDROANTHUS IMPETIGINOSUS BARK, PICEA MARIANA RESIN, SODIUM BORATE, LYCOPODIUM CLAVATUM SPORE, STRYCHNOS NUX-VOMICA SEED, PHOSPHORUS, PULSATILLA VULGARIS WHOLE, SEPIA OFFICINALIS JUICE, THUJA OCCIDENTALIS LEAFY TWIG, SKATOLE, CANDIDA ALBICANS |
| 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], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC] and 3 more |
| Marketing start | Mar 8, 2024 |
| 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: