NDC product
Thyroid HP
NDC 44911-0057 · Energique, Inc.
Key facts
| Product NDC | 44911-0057 |
|---|---|
| Proprietary name | Thyroid HP |
| Nonproprietary name | Baryta Carbonica, Calcarea Carbonica, Calcarea Iodata, Fucus Vesiculosus, Iodium, Natrum Muriaticum, Pulsatilla (Vulgaris), Spongia Tosta, Thyroidinum (Suis) |
| Substances | BARIUM CARBONATE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, CALCIUM IODIDE, FUCUS VESICULOSUS, IODINE, SODIUM CHLORIDE, PULSATILLA VULGARIS WHOLE, SPONGIA OFFICINALIS SKELETON, ROASTED, THYROID |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Energique, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC] and 1 more |
| Marketing start | Dec 3, 2012 |
| Marketing end | Aug 26, 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