NDC product
Matervia
NDC 72835-660 · V2 Pharma LLC
Key facts
| Product NDC | 72835-660 |
|---|---|
| Proprietary name | Matervia |
| Nonproprietary name | ascorbic acid, cholecalciferol, thiamine, pyridoxal-5-phosphate, folic acid, methylcobalamin, calcium citrate, iron, iodine |
| Substances | ASCORBIC ACID, CHOLECALCIFEROL, THIAMINE MONONITRATE, PYRIDOXAL 5-PHOSPHATE, FOLIC ACID, METHYLCOBALAMIN, CALCIUM CITRATE, IRON, POTASSIUM IODIDE |
| Dosage form | CAPSULE |
| Route | ORAL |
| Labeler | V2 Pharma LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Pharmacologic classes | Ascorbic Acid [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE] and 5 more |
| Marketing start | Jun 11, 2025 |
| 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: