NDC product
Dialyvite 5000
NDC 10542-011 · Hillestad Pharmaceuticals USA
Key facts
| Product NDC | 10542-011 |
|---|---|
| Proprietary name | Dialyvite 5000 |
| Nonproprietary name | Ascorbic Acid, Tocopheryl Acid Succinate, Thiamine, Riboflavin, Niacinamide, Pyridoxine, Folic Acid, Cobalamin, Biotin, Pantothenic Acid, Zinc, Selenium |
| Substances | ASCORBIC ACID, THIAMINE MONONITRATE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, COBALAMIN, BIOTIN, CALCIUM PANTOTHENATE, ZINC CITRATE, .ALPHA.-TOCOPHEROL SUCCINATE, D-, SELENOCYSTEINE |
| Dosage form | TABLET, COATED |
| Route | ORAL |
| Labeler | Hillestad Pharmaceuticals USA |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Pharmacologic classes | Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC] and 1 more |
| Marketing start | May 1, 2008 |
| Marketing end | Feb 28, 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