NDC product
Histatone
NDC 44911-0580 · Energique, Inc.
Key facts
| Product NDC | 44911-0580 |
|---|---|
| Proprietary name | Histatone |
| Nonproprietary name | Allium Sativum, Baptisia Tinctoria, Echinacea (Angustifolia), Allium Cepa, Ambrosia Artemisiaefolia, Arsenicum Album, Phosphorus, Pulsatilla (Pratensis), Solidago Virgaurea |
| Substances | GARLIC, BAPTISIA TINCTORIA ROOT, ECHINACEA ANGUSTIFOLIA WHOLE, ONION, AMBROSIA ARTEMISIIFOLIA WHOLE, ARSENIC TRIOXIDE, PHOSPHORUS, PULSATILLA PRATENSIS WHOLE, SOLIDAGO VIRGAUREA FLOWERING TOP |
| 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], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Plant Proteins [CS] and 1 more |
| Marketing start | May 25, 2021 |
| 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: