NDC product
Progenite
NDC 43742-2126 · Deseret Biologicals
Key facts
| Product NDC | 43742-2126 |
|---|---|
| Proprietary name | Progenite |
| Nonproprietary name | Ammonium Carbonicum, Baryta Muriatica, Borax, Caulophyllum Thalictroides, Natrum Carbonicum, Sabal Serrulata, Sabina, Sulphuricum Acidum, Thiosinaminum, Folliculinum, Tuba Uterina Suis, Uterus Suis and 9 more |
| Substances | AMMONIUM CARBONATE, BARIUM CHLORIDE DIHYDRATE, SODIUM BORATE, CAULOPHYLLUM THALICTROIDES ROOT, SODIUM CARBONATE, SAW PALMETTO, JUNIPERUS SABINA LEAFY TWIG, SULFURIC ACID, ALLYLTHIOUREA, ESTRONE, SUS SCROFA FALLOPIAN TUBE, SUS SCROFA UTERUS and 9 more |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Deseret Biologicals |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | Dec 21, 2023 |
| 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: