NDC product
Oxaltem
NDC 75053-0009 · Nucleic Products, LLC
Key facts
| Product NDC | 75053-0009 |
|---|---|
| Proprietary name | Oxaltem |
| Nonproprietary name | Berberis Vulgaris, Oxalicum Acidum, Sanguinaria Canadensis, Chimaphila Umbellata, Calcarea Fluorica, Calcarea Silicata, Uricum Acidum, Calcarea Phosphorica, Parathormonum, Pyridoxinum Hydrochloricum |
| Substances | BERBERIS VULGARIS ROOT BARK, OXALIC ACID, SANGUINARIA CANADENSIS WHOLE, CHIMAPHILA UMBELLATA WHOLE, CALCIUM FLUORIDE, CALCIUM SILICATE, URIC ACID, TRIBASIC CALCIUM PHOSPHATE, PARATHYROID HORMONE, PYRIDOXINE HYDROCHLORIDE |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Nucleic Products, LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Analogs/Derivatives [Chemical/Ingredient], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE] and 6 more |
| Marketing start | Jan 31, 2022 |
| Marketing end | Jul 26, 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