NDC product
PARATHYROID CORD
NDC 44911-0212 · Energique, Inc.
Key facts
| Product NDC | 44911-0212 |
|---|---|
| Proprietary name | PARATHYROID CORD |
| Nonproprietary name | Parathyroid gland (suis) |
| Substances | SUS SCROFA PARATHYROID GLAND |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Energique, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | Jul 16, 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: