NDC product
Vitafol One
NDC 0642-0070 · Exeltis USA, Inc.
Key facts
| Product NDC | 0642-0070 |
|---|---|
| Proprietary name | Vitafol |
| Nonproprietary name | Prenatal Supplement with DHA |
| Substances | VITAMIN A, ASCORBIC ACID, THIAMINE MONONITRATE, RIBOFLAVIN, NIACIN, PYRIDOXINE HYDROCHLORIDE, CYANOCOBALAMIN, FOLIC ACID, IODINE, MAGNESIUM, ZINC, COPPER and 4 more |
| Dosage form | CAPSULE, GELATIN COATED |
| Route | ORAL |
| Labeler | Exeltis USA, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Pharmacologic classes | Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE] and 15 more |
| Marketing start | Jun 13, 2011 |
| 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: