NDC product
Diatrol
NDC 59088-162 · PureTek Corporation
Key facts
| Product NDC | 59088-162 |
|---|---|
| Proprietary name | Diatrol |
| Nonproprietary name | vitamins and mineral |
| Substances | BIOTIN, VANADYL SULFATE, CHROMIUM NICOTINATE, GYMNEMA SYLVESTRE LEAF, ARGININE HYDROCHLORIDE, .ALPHA.-TOCOPHEROL ACETATE, DL-, PHYTONADIONE, VITAMIN A, ASCORBIC ACID, CHOLECALCIFEROL, PYRIDOXINE HYDROCHLORIDE, THIAMINE MONONITRATE and 5 more |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | PureTek Corporation |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Pharmacologic classes | Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Folate Analog [EPC], Folic Acid [CS], Increased Prothrombin Activity [PE], Reversed Anticoagulation Activity [PE] and 10 more |
| Marketing start | Jan 26, 2024 |
| 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: