NDC product
DIANEAL LOW CALCIUM WITH DEXTROSE
NDC 0941-0711 · Vantive US Healthcare LLC
Key facts
| Product NDC | 0941-0711 |
|---|---|
| Proprietary name | DIANEAL LOW CALCIUM WITH DEXTROSE |
| Nonproprietary name | sodium chloride, sodium lactate, calcium chloride, magnesium chloride and dextrose |
| Substances | DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE |
| Dosage form | INJECTION, SOLUTION |
| Route | INTRAPERITONEAL |
| Labeler | Vantive US Healthcare LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
| Pharmacologic classes | Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE] and 9 more |
| Marketing start | Oct 23, 2024 |
| Marketing end | Oct 17, 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