NDC product
Lipostat
NDC 44911-0358 · Energique, Inc.
Key facts
| Product NDC | 44911-0358 |
|---|---|
| Proprietary name | Lipostat |
| Nonproprietary name | Capsicum Annuum, Fucus Vesiculosus, Borage Officinalis, Lecithin, Calcarea Carbonica, Ferrum Metallicum, Kali Bichromicum, Kali Carbonica, Pulsatilla (Pratensis), Sulphur |
| Substances | CAPSICUM, FUCUS VESICULOSUS, BORAGE, EGG PHOSPHOLIPIDS, OYSTER SHELL CALCIUM CARBONATE, CRUDE, IRON, POTASSIUM DICHROMATE, POTASSIUM CARBONATE, PULSATILLA PRATENSIS WHOLE, SULFUR |
| 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], Non-Standardized Plant Allergenic Extract [EPC] and 2 more |
| Marketing start | May 6, 2016 |
| 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: