NDC product
Vitafol-OB Plus DHA Prenatal Supplement Plus DHA
NDC 0642-0076 · Exeltis USA, Inc
Key facts
| Product NDC | 0642-0076 |
|---|---|
| Proprietary name | Vitafol-OB Plus DHA |
| Nonproprietary name | Vitamin A, Ascorbic Acid, Vitamin D, .Alpha.-Tocopherol, Thiamine Mononitrate, Riboflavin, Niacin, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, Calcium, Iron and 4 more |
| Dosage form | KIT |
| Labeler | Exeltis USA, Inc |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing start | Feb 16, 2007 |
| 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: