NDC product
Age Defiance Pro
NDC 44911-0474 · Energique, Inc.
Key facts
| Product NDC | 44911-0474 |
|---|---|
| Proprietary name | Age Defiance Pro |
| Nonproprietary name | 7-Oxo-Dehydroepiandrosterone-3B-Acetate, Calcarea Carbonica, Conium Maculatum, Glandula Suprarenalis Suis, Hepar Suis, Hydrofluoricum Acidum, Hypophysis Suis, Lycopodium Clavatum, Selenium Metallicum, Sepia, Silicea, Human Growth Hormone |
| Substances | 7-OXODEHYDROEPIANDROSTERONE 3-ACETATE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, CONIUM MACULATUM FLOWERING TOP, SUS SCROFA ADRENAL GLAND, PORK LIVER, HYDROFLUORIC ACID, SUS SCROFA PITUITARY GLAND, LYCOPODIUM CLAVATUM SPORE, SELENIUM, SEPIA OFFICINALIS JUICE, SILICON DIOXIDE, SOMATROPIN |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Energique, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Human Growth Hormone [CS], Recombinant Human Growth Hormone [EPC] |
| Marketing start | Sep 24, 2018 |
| Marketing end | Dec 11, 2028 |
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