NDC product
Concept DHA
NDC 52747-621 · U.S. Pharmaceutical Corporation
Key facts
| Product NDC | 52747-621 |
|---|---|
| Proprietary name | Concept DHA |
| Nonproprietary name | Vitamin- Mineral Omega-3 Supplement |
| Substances | FERROUS FUMARATE, IRON, ASCORBIC ACID, FOLIC ACID, THIAMINE MONONITRATE, RIBOFLAVIN, NIACIN, CALCIUM PANTOTHENATE, PYRIDOXINE HYDROCHLORIDE, BIOTIN, CYANOCOBALAMIN, CUPRIC SULFATE and 3 more |
| Dosage form | CAPSULE, LIQUID FILLED |
| Route | ORAL |
| Labeler | U.S. Pharmaceutical Corporation |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Pharmacologic classes | Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Calculi Dissolution Agent [EPC], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Fatty Acids and 16 more |
| Marketing start | Jun 24, 2009 |
| Listing certified through | Dec 31, 2026 |
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: