NDC product
Cholenest
NDC 60986-1008 · Marco Pharma International LLC.
Key facts
| Product NDC | 60986-1008 |
|---|---|
| Proprietary name | Cholenest |
| Nonproprietary name | Rhamnus purshiana, Carduus marianus, Taraxacum officinale, Chelidonium majus, Leptandra virginica, Myrica cerifera, Berberis vulgaris, Natrum sulphuricum, Magnesia phosphorica, Cuprum metallicum |
| Substances | FRANGULA PURSHIANA BARK, SILYBUM MARIANUM SEED, TARAXACUM OFFICINALE, CHELIDONIUM MAJUS, VERONICASTRUM VIRGINICUM ROOT, MORELLA CERIFERA ROOT BARK, BERBERIS VULGARIS ROOT BARK, SODIUM SULFATE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, COPPER |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Marco Pharma International LLC. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Calculi Dissolution Agent [EPC], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Large Intestinal Motility [PE] and 7 more |
| Marketing start | Mar 1, 1992 |
| Listing certified through | Dec 31, 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 · Source date: